Symkevi 50 mg/75 mg film coated tablets

Symkevi is indicated in a combination regimen with ivacaftor tablets for the treatment of patients with cystic fibrosis (CF) aged 6 years and older who are homozygous for the F508del mutation or who are heterozygous for the F508del mutation and have one of the following mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: P67L, R117C, L206W, R352Q, A455E, D579G, 711+3A→ G, S945L, S977F, R1070W, D1152H, 2789+5G→ A, 3272-26A→ G, and 3849+10kbC→ T.

Symkevi should only be prescribed by physicians with experience in the treatment of CF. If the patient's genotype is unknown, an accurate and validated genotyping method should be performed to confirm the presence of an indicated mutation using a genotyping assay.

Posology

Adults, adolescents and children aged 6 years and older should be dosed according to Table 1.

The morning and evening dose should be taken approximately 12 hours apart with fat-containing food (see Method of administration).

Missed dose

If 6 hours or less have passed since the missed morning or evening dose, the patient should take the missed dose as soon as possible and continue on the original schedule.

If more than 6 hours have passed since the missed morning or evening dose, the patient should not take the missed dose. The next scheduled dose can be taken at the usual time.

More than one dose of either tablet should not be taken at the same time.

Concomitant use of CYP3A inhibitors

The dose of Symkevi and ivacaftor should be adjusted when co-administered with moderate and strong CYP3A inhibitors.

When co-administered with moderate CYP3A inhibitors (e.g., fluconazole, erythromycin, verapamil), or strong CYP3A inhibitors (e.g., ketoconazole, itraconazole, posaconazole, voriconazole, telithromycin, and clarithromycin), the dose should be reduced according to Table 2 (see sections 4.4 and 4.5).

Special populations

Elderly people

The safety, efficacy and pharmacokinetics of Symkevi have been examined in a limited number of elderly patients. No dose adjustment specific to this patient population is required (see section 5.2).

Renal impairment

No dose adjustment is recommended for patients with mild or moderate renal impairment. Caution is recommended in patients with severe renal impairment or end-stage renal disease (see sections 4.4 and 5.2).

Hepatic impairment

For dose adjustment for patients with hepatic impairment, (see Table 3). There is no experience of the use of Symkevi in patients with severe hepatic impairment (Child-Pugh Class C); therefore, its use is not recommended unless the benefits outweigh the risks. In such cases, Symkevi should be used at a reduced dose (see sections 4.4 and 5.2). No dose adjustment is necessary for Symkevi in patients with mild hepatic impairment (Child-Pugh Class A).

Paediatric population

The safety and efficacy of Symkevi in children aged less than 6 years has not yet been established. No data are available (see sections 4.8 and 5.1).

Method of administration

For oral use.

Patients should be instructed to swallow the tablets whole. The tablets should not be chewed, crushed, or broken before swallowing because there are no clinical data currently available to support other methods of administration.

Both Symkevi and ivacaftor tablets should be taken with fat-containing food, such as food recommended in standard nutritional guidelines (see section 5.2).

Food or drink containing grapefruit should be avoided during treatment (see section 4.5).

Hypersensitivity to the active substances or to any of the excipients listed in section 6.1.

Symkevi should not be prescribed in patients with CF who are heterozygous for the F508del mutation and have a second CFTR mutation not listed in section 4.1.

Elevated transaminase and hepatic injury

Liver function decompensation, including liver failure leading to transplantation and death has been reported in CF patients with pre-existing cirrhosis and portal hypertension whilst receiving treatment with other CFTR modulator regimens. TEZ/IVA in combination with IVA should be used with caution in patients with advanced liver disease and only if the benefits are expected to outweigh the risks. If TEZ/IVA is used in these patients they should be closely monitored after the initiation of treatment (see sections 4.2, 4.8 and 5.2).

Elevated transaminases are common in patients with CF and have been observed in some patients treated with Symkevi in combination with ivacaftor, as well as with ivacaftor monotherapy. Therefore, liver function tests are recommended for all patients prior to initiating treatment, every 3 months during the first year of treatment, and annually thereafter. For patients with a history of transaminase elevations, more frequent monitoring of liver function tests should be considered. In the event of significant elevations of transaminases (e.g., patients with ALT or AST >5 x the upper limit of normal (ULN), or ALT or AST >3 x ULN with bilirubin >2 x ULN), dosing should be interrupted and laboratory tests closely followed until the abnormalities resolve. Following resolution of transaminase elevations, the benefits and risks of resuming treatment should be considered (see section 4.8).

Hepatic impairment

The use of Symkevi is not recommended in patients with severe hepatic impairment unless the benefits are expected to outweigh the risks (see sections 4.2 and 5.2).

Renal impairment

Caution is recommended in patients with severe renal impairment or end-stage renal disease (see sections 4.2 and 5.2).

Patients after organ transplantation

Symkevi in combination with ivacaftor has not been studied in patients with CF who have undergone organ transplantation. Therefore, use in transplanted patients is not recommended. See section 4.5 for interactions with ciclosporin or tacrolimus.

Interactions with medicinal products

CYP3A inducers

Exposure to tezacaftor and ivacaftor may be reduced by the concomitant use of CYP3A inducers, potentially resulting in reduced efficacy of Symkevi and ivacaftor. Therefore, co-administration with strong CYP3A inducers is not recommended (see section 4.5).

CYP3A inhibitors

The dose of Symkevi and ivacaftor should be adjusted when used concomitantly with strong or moderate CYP3A inhibitors (see section 4.5 and Table 2 in section 4.2).

Paediatric population

Cataracts

Cases of non-congenital lens opacities without impact on vision have been reported in paediatric patients treated with ivacaftor-containing regimens. Although other risk factors were present in some cases (such as corticosteroid use and exposure to radiation), a possible risk attributable to treatment cannot be excluded. Baseline and follow-up ophthalmological examinations are recommended in paediatric patients initiating treatment with Symkevi in combination with ivacaftor (see section 5.3).

Sodium content

This medicinal product contains less than 1 mmol sodium (23 mg) per dose, that is to say essentially 'sodium-free'.

Medicinal products affecting the pharmacokinetics of tezacaftor and ivacaftor

CYP3A inducers

Tezacaftor and ivacaftor are substrates of CYP3A (ivacaftor is a sensitive substrate of CYP3A). Concomitant use of CYP3A inducers may result in reduced exposures and thus reduced efficacy of Symkevi and ivacaftor. Co-administration of ivacaftor with rifampicin, a strong CYP3A inducer, significantly decreased ivacaftor exposure [area under the curve (AUC)] by 89%. Tezacaftor exposures can also be expected to decrease significantly during co-administration with strong CYP3A inducers; therefore, co-administration with strong CYP3A inducers is not recommended.

Examples of strong CYP3A inducers include rifampicin, rifabutin, phenobarbital, carbamazepine, phenytoin, and St. John's wort (Hypericum perforatum).

CYP3A inhibitors

Co-administration with itraconazole, a strong CYP3A inhibitor, increased tezacaftor exposure (measured as AUC) by 4-fold and increased ivacaftor AUC by 15.6-fold. The dose of Symkevi should be adjusted when co-administered with strong CYP3A inhibitors (see Table 2 in section 4.2).

Examples of strong CYP3A inhibitors include ketoconazole, itraconazole, posaconazole, and voriconazole, telithromycin and clarithromycin.

Physiologically based pharmacokinetic modeling suggested co-administration with fluconazole, a moderate CYP3A inhibitor, may increase tezacaftor exposure (AUC) by approximately 2-fold. Co-administration of fluconazole increased ivacaftor AUC by 3-fold. The dose of Symkevi and ivacaftor should be adjusted when co-administered with moderate CYP3A inhibitors (see Table 2 in section 4.2).

Examples of moderate CYP3A inhibitors include fluconazole, erythromycin and verapamil.

Co-administration with grapefruit juice, which contains one or more components that moderately inhibit CYP3A, may increase exposure of ivacaftor and tezacaftor; therefore, food or drink containing grapefruit should be avoided during treatment (see section 4.2).

Potential for tezacaftor/ivacaftor to interact with transporters

In vitro studies showed that tezacaftor is a substrate for the uptake transporter OATP1B1, and efflux transporters P-glycoprotein (P-gp) and Breast Cancer Resistance Protein (BCRP). Tezacaftor is not a substrate for OATP1B3. Exposure to tezacaftor is not expected to be affected significantly by concomitant inhibitors of OATP1B1, P-gp, or BCRP due to its high intrinsic permeability and low likelihood of being excreted intact. However, exposure to M2-TEZ (tezacaftor metabolite) may be increased by inhibitors of P-gp. Therefore, caution should be used when P-gp inhibitors are used with Symkevi.

In vitro studies showed that ivacaftor is not a substrate for OATP1B1, OATP1B3, or P-gp. Ivacaftor and its metabolites are substrates of BCRP in vitro. Due to its high intrinsic permeability and low likelihood of being excreted intact, co-administration of BCRP inhibitors is not expected to alter exposure of ivacaftor and M1-IVA, while any potential changes in M6-IVA exposures are not expected to be clinically relevant.

Ciprofloxacin

Co-administration of ciprofloxacin did not affect the exposure of ivacaftor or tezacaftor. No dose adjustment is required when Symkevi is co-administered with ciprofloxacin.

Medicinal products affected by tezacaftor and ivacaftor

CYP2C9 substrates

Ivacaftor may inhibit CYP2C9; therefore, monitoring of the international normalized ratio (INR) is recommended during co-administration of warfarin with Symkevi given in combination with ivacaftor. Other medicinal products for which exposure may be increased include glimepiride and glipizide; these medicinal products should be used with caution.

CYP3A, digoxin and other P-gp substrates

CYP3A substrates

Co-administration with (oral) midazolam, a sensitive CYP3A substrate, did not affect midazolam exposure. No dose adjustment of CYP3A substrates is required when co-administered with Symkevi in combination with ivacaftor.

Digoxin and other P-gp substrates

Co-administration with digoxin, a sensitive P-gp substrate, increased digoxin exposure by 1.3-fold, consistent with weak inhibition of P-gp by ivacaftor. Administration of Symkevi in combination with ivacaftor may increase systemic exposure of medicinal products that are sensitive substrates of P-gp, which may increase or prolong their therapeutic effect and adverse reactions. When used concomitantly with digoxin or other substrates of P-gp with a narrow therapeutic index, such as ciclosporin, everolimus, sirolimus, and tacrolimus, caution and appropriate monitoring should be used.

Hormonal contraceptives

Symkevi in combination with ivacaftor has been studied with an estrogen/progesterone oral contraceptive and was found to have no significant effect on the exposures of the hormonal contraceptive. Symkevi and ivacaftor are not expected to modify the efficacy of hormonal contraceptives.

OATP1B1 substrates

Symkevi in combination with ivacaftor has been studied with pitavastatin, an OATP1B1 substrate, and was found to have no clinically relevant effect on the exposure of pitavastatin (1.24-fold increased exposure based on AUC). No dose adjustment of OATP1B1 substrates is required when co-administered with Symkevi.

Paediatric population

Interaction studies have only been performed in adults.

Pregnancy

There are no or limited amount of data (less than 300 pregnancy outcomes) from the use of tezacaftor or ivacaftor in pregnant women. Animal studies do not indicate direct or indirect harmful effects with respect to reproductive toxicity (see section 5.3). As a precautionary measure, it is preferable to avoid the use of therapy during pregnancy.

Breast-feeding

It is unknown whether tezacaftor, ivacaftor, or their metabolites are excreted in human milk. Available pharmacokinetic/toxicological data in animals have shown excretion of tezacaftor and ivacaftor into the milk of lactating female rats (see section 5.3). A risk to the newborns/infants cannot be excluded. A decision must be made whether to discontinue breast-feeding or to discontinue/abstain from therapy taking into account the benefit of breast-feeding for the child and the benefit of therapy for the woman.

Fertility

Tezacaftor

There are no data available on the effect of tezacaftor on fertility in humans. Tezacaftor had no effects on fertility and reproductive performance indices in male and female rats at doses up to 100 mg/kg/day.

Ivacaftor

There are no data available on the effect of ivacaftor on fertility in humans. Ivacaftor had an effect on fertility in rats (see section 5.3).

Symkevi in combination with ivacaftor has minor influence on the ability to drive and use machines. Dizziness has been reported in patients receiving Symkevi in combination with ivacaftor, as well as ivacaftor monotherapy (see section 4.8). Patients experiencing dizziness should be advised not to drive or use machines until symptoms abate.

Summary of the safety profile

The most common adverse reactions experienced by patients aged 12 years and older who received Symkevi in combination with ivacaftor in phase 3 clinical studies were headache (14% versus 11% on placebo) and nasopharyngitis (12% versus 10% on placebo).

Tabulated list of adverse reactions

Table 4 reflects adverse reactions observed with Symkevi in combination with ivacaftor and with ivacaftor monotherapy in clinical studies. Adverse reactions are listed by MedDRA system organ class and frequency: very common (≥ 1/ 10); common (≥ 1/ 100 to <1/ 10); uncommon (≥ 1/ 1 000 to <1/ 100); rare (≥ 1/ 10 000 to <1/ 1 000); very rare (<1/ 10 000); not known (cannot be estimated from the available data).

The safety data from 1042 adults and 130 children aged 6 to less than 12 years old, treated with Symkevi in combination with ivacaftor for up to an additional 96 weeks in two long-term safety and efficacy rollover studies (study 661-110 and study 661-116 part A, respectively) were consistent with the safety data from the placebo-controlled phase 3 studies.

Description of selected adverse reactions

Transaminase elevations

During the adult placebo-controlled phase 3 studies (up to 24 weeks), the incidence of maximum transaminase (ALT or AST) >8, >5, or >3 x ULN were similar between Symkevi- and placebo-treated patients; 0.2%, 1.0%, and 3.4% in Symkevi-treated patients, and 0.4%, 1.0%, and 3.4% in placebo-treated patients. One patient (0.2%) on therapy and two patients (0.4%) on placebo permanently discontinued treatment for elevated transaminases. No patients treated with Symkevi experienced a transaminase elevation >3 x ULN associated with elevated total bilirubin >2 x ULN.

Paediatric population

The safety of Symkevi in combination with ivacaftor was evaluated in 124 patients between 6 to less than 12 years of age. The tezacaftor 100 mg/ivacaftor 150 mg and ivacaftor 150 mg dose has not been investigated in clinical studies in children aged 6 to less than 12 years weighing 30 to < 40 kg.

The safety profile is generally consistent among children and adolescents, and is also consistent with adult patients.

During the 24-week, open-label phase 3 study in patients aged 6 to less than 12 years (study 661-113 part B, n=70), the incidence of maximum transaminase (ALT or AST) >8, >5, and >3 x ULN were 1.4%, 4.3%, and 10.0%, respectively. No Symkevi-treated patients experienced a transaminase elevation >3 x ULN associated with elevated total bilirubin >2 x ULN or discontinued Symkevi treatment due to transaminase elevations. One patient interrupted treatment due to elevated transaminases, and subsequently resumed Symkevi treatment successfully (see section 4.4 for management of elevated transaminases).

Other special populations

The safety profile of Symkevi in combination with ivacaftor, including respiratory events (e.g., chest discomfort, dyspnea, and respiration abnormal), was generally similar across all subgroups of patients, including analysis by age, gender, and baseline percent predicted FEV₁ (ppFEV₁).

Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via:

Yellow Card Scheme

Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.

There are no known risks due to overdose with Symkevi and there is no specific antidote available in the event of overdose. Treatment of overdose consists of general supportive measures including monitoring of vital signs and observation of the clinical status of the patient.

Pharmacotherapeutic group: Other respiratory system products; ATC code: R07AX31

Mechanism of action

Tezacaftor is a selective CFTR corrector that binds to the first Membrane Spanning Domain (MSD-1) of CFTR. Tezacaftor facilitates the cellular processing and trafficking of normal or multiple mutant forms of CFTR (including F508del-CFTR) to increase the amount of CFTR protein delivered to the cell surface, resulting in increased chloride transport in vitro.

Ivacaftor is a CFTR potentiator that potentiates the channel-open probability (or gating) of CFTR at the cell surface to increase chloride transport. For ivacaftor to function CFTR protein must be present at the cell surface. Ivacaftor can potentiate the CFTR protein delivered to the cell surface by tezacaftor, leading to a further enhancement of chloride transport than either active substance alone. The combination targets the abnormal CFTR protein by increasing the quantity and function of CFTR at the cell surface and subsequently increasing airway surface liquid height, and ciliary beat frequency in vitro in human bronchial epithelial (HBE) cells from homozygous F508del CF patients. The exact mechanisms by which tezacaftor improves cellular processing and trafficking of F508del-CFTR and ivacaftor potentiates F508del-CFTR are not known.

Pharmacodynamic effects

Effects on sweat chloride

In study 661-106 (patients homozygous for the F508del mutation), the treatment difference between Symkevi in combination with ivacaftor and placebo in mean absolute change from baseline in sweat chloride through week 24 was -10.1 mmol/L (95% CI: -11.4, -8.8; nominal P<0.0001^*).

In study 661-108 (patients heterozygous for the F508del mutation and a second mutation associated with residual CFTR activity), the treatment difference in mean absolute change from baseline in sweat chloride through week 8 was -9.5 mmol/L (95% CI: -11.7, -7.3; nominal P<0.0001^*) between Symkevi in combination with ivacaftor and placebo, and -4.5 mmol/L (95% CI: -6.7, -2.3; nominal P<0.0001^*) between ivacaftor and placebo.

In study 661-115 (patients aged 6 to less than 12 years who were homozygous or heterozygous for the F508del mutation and a second mutation associated with residual CFTR activity), the within treatment mean absolute change in sweat chloride from baseline at week 8 was -12.3 mmol/L (95% CI: -15.3, -9.3; nominal P<0.0001). In subgroup analyses the mean absolute change was -12.9 mmol/L (95% CI: -16.0, -9.9) for patients with F/F and for patients with F/RF the mean absolute change was -10.9 mmol/L (95% CI: -20.8, -0.9).

^*Nominal p-value, based on hierarchical testing procedure.

In study 661-116 part A patients (aged 6 years and older) rolled over from studies 661-113 part B and 661-115. The changes observed in sweat chloride in study 661-113 part B and 661-115 were maintained over 96 weeks of treatment with Symkevi in combination with ivacaftor. At week 96, the LS mean absolute change from parent baseline in sweat chloride for patients from study 661-113 part B was -16.2 mmol/L (95% CI: -21.9, -10.5), and for patients from study 661-115 was -13.8 mmol/L (95% CI: -17.7, -9.9).

ECG evaluation

Neither tezacaftor nor ivacaftor prolong the QTcF interval in healthy subjects at 3 times the therapeutic dose.

Clinical efficacy and safety

The efficacy of Symkevi in combination with ivacaftor 150 mg tablet in adult and adolescent patients with CF was demonstrated in two phase 3, double-blind, controlled studies (study 661-106 and study 661-108), and one phase 3, open-label extension study (study 661-110).

Study 661-106 was a 24-week, randomised, double-blind, placebo-controlled study. A total of 504 patients aged 12 years and older (mean age 26.3 years) who were homozygous for the F508del mutation in the CFTR gene were randomised (1:1 randomization: 248 Symkevi in combination with ivacaftor, 256 placebo). Patients had a percent predicted forced expiratory volume in one second (ppFEV₁) at screening between 40 to 90%. The mean ppFEV₁ at baseline was 60.0% (range: 27.8% to 96.2%).

Study 661-108 was a randomised, double-blind, placebo-controlled, 2-period, 3-treatment, 8-week crossover study. A total of 244 patients aged 12 years and older (mean age 34.8 years) who were heterozygous for the F508del mutation and a second mutation associated with residual CFTR activity were randomised to and received sequences of treatment that included Symkevi in combination with ivacaftor, ivacaftor, and placebo. Patients had a ppFEV₁ at screening between 40 to 90%. The mean ppFEV₁ at baseline was 62.3% (range: 34.6% to 93.5%).

Patients in studies 661-106 and 661-108 continued on their standard-of-care CF therapies during the studies (e.g., bronchodilators, inhaled antibiotics, dornase alfa, and hypertonic saline), and were eligible to rollover into a 96-week open-label extension study (study 661-110). Patients had a confirmed genotype of a protocol-specified CFTR mutation, and a confirmed diagnosis of CF.

Patients with a history of colonization with organisms associated with a more rapid decline in pulmonary status such as Burkholderia cenocepacia, Burkholderia dolosa, or Mycobacterium abscessus, or who had two or more abnormal liver function tests at screening (ALT, AST, AP, GGT ≥ 3 x ULN or total bilirubin ≥ 2 x ULN) or AST or ALT ≥ 5 x ULN, were excluded from both studies.

Study 661-106

In study 661-106 treatment with Symkevi in combination with ivacaftor resulted in a statistically significant improvement in ppFEV₁ (see Table 5). The treatment difference between Symkevi (in combination with ivacaftor) and placebo for the primary endpoint of mean absolute change (95% CI) in ppFEV₁ from baseline through week 24 was 4.0 percentage points (95% CI: 3.1, 4.8; P<0.0001). Mean improvement in ppFEV₁ was observed at the first assessment on day 15 and sustained throughout the 24-week treatment period. Improvements in ppFEV₁ were observed regardless of age, sex, baseline ppFEV₁, colonization with Pseudomonas, concomitant use of standard-of-care therapies for CF, and geographic region. See Table 5 for a summary of primary and key secondary outcomes.

Symkevi in combination with ivacaftor was associated with a lower event rate per year of severe pulmonary exacerbations requiring hospitalization or intravenous antibiotic therapy (0.29) compared to placebo (0.54). The rate ratio versus placebo was 0.53 (95% CI: 0.34, 0.82; nominal P= 0.0042). Pulmonary exacerbations requiring intravenous antibiotic therapy were lower in the treatment group compared to placebo (RR: 0.53 [95% CI: 0.34, 0.82]; nominal P=0.0042). Pulmonary exacerbations requiring hospitalizations were similar between treatment groups (RR: 0.78 [95% CI: 0.44, 1.36]; P=0.3801).

BMI increased in both treatment groups (Symkevi in combination with ivacaftor: 0.18 kg/m², placebo: 0.12 kg/m²). The treatment difference of 0.06 kg/m² for mean change in BMI from baseline to week 24 (95% CI: -0.08, 0.19) was not statistically significant (P=0.4127).

For CFQ-R respiratory domain score (a measure of respiratory symptoms relevant to patients with CF including cough, sputum production, and difficulty breathing) the percentage of subjects with at least a 4 point-increase from baseline (minimal clinically important difference) was 51.1% for Symkevi and 35.7% for placebo at week 24.

Study 661-108

Of the 244 patients enrolled in study 661-108 the following indicated mutations associated with residual CFTR activity were represented: P67L, R117C, L206W, R352Q, A455E, D579G, 711+3A→ G, S945L, S977F, R1070W, D1152H, 2789+5G→ A, 3272-26A→ G, and 3849+10kbC→ T.

In study 661-108 treatment with Symkevi in combination with ivacaftor resulted in a statistically significant improvement in ppFEV₁ (see Table 6). The treatment difference between Symkevi in combination with ivacaftor- and placebo-treated patients for the primary endpoint of mean absolute change in ppFEV₁ from study baseline to the average of week 4 and week 8 was 6.8 percentage points (95% CI: 5.7, 7.8; P<0.0001). The treatment difference between ivacaftor alone- and placebo-treated patients was 4.7 percentage points (95% CI: 3.7, 5.8; P<0.0001) and 2.1 percentage points (95% CI: 1.2, 2.9) between Symkevi in combination with ivacaftor- and ivacaftor alone-treated patients. Mean improvement in ppFEV₁ was observed at the first assessment on day 15 and sustained throughout the 8-week treatment period. Improvements in ppFEV₁ were observed regardless of age, disease severity, sex, mutation class, colonization with Pseudomonas, concomitant use of standard-of-care therapies for CF, and geographic region. See Table 6 for a summary of primary and key secondary outcomes.

Subgroup analysis of patients with severe lung dysfunction (ppFEV₁ <40)

Study 661-106 and study 661-108 included a total of 39 patients treated with Symkevi in combination with ivacaftor with ppFEV₁ <40. There were 23 patients with ppFEV₁ <40 at baseline receiving Symkevi and 24 patients receiving placebo in study 661-106. The mean treatment difference between Symkevi and placebo-treated patients for absolute change in ppFEV₁ through week 24 in this subgroup was 3.5 percentage points (95% CI: 1.0, 6.1). There were 16 patients with ppFEV₁ <40 at baseline receiving Symkevi, 13 receiving ivacaftor and 15 receiving placebo in study 661-108. The mean treatment difference between Symkevi and placebo-treated patients for absolute change in ppFEV₁ through the average of week 4 and week 8 was 4.4 percentage points (95% CI: 1.1, 7.8). The mean treatment difference between ivacaftor and placebo-treated patients was 4.4 percentage points (95% CI: 0.9, 7.9).

Study 661-110

Study 661-110 was a phase 3, open-label, multicenter, rollover, 96-week study to evaluate the safety and efficacy of long-term treatment with Symkevi in combination with ivacaftor in patients from studies 661-106 (n=462) and 661-108 (n=227). Efficacy was a secondary objective for study 661-110 and the efficacy endpoints were not adjusted for multiplicity.

Patients who received placebo in both study 661-106 and study 661-108 demonstrated improvements in ppFEV₁ when treated with Symkevi in combination with ivacaftor in study 661-110 [study 661-106: within-group change=2.1(95% CI: 0.8, 3.3) percentage points, study 661-108: within-group change=4.1 (95% CI: 2.2, 6.0) percentage points]. Patients who received Symkevi in combination with ivacaftor in the parent studies and continued on treatment, showed a slight attenuation in ppFEV₁ in the extension study, however the overall treatment effect was still positive through 120 weeks and 104 weeks for study 661-106 and study 661-108, respectively.

Similar trends were observed for CFQ-R respiratory domain score, pulmonary exacerbation rate and BMI.

Paediatric population

Adolescents aged 12 years and older

Adolescents were included together with adults in the studies.

Adolescent patients with CF who were homozygous for the F508del mutation in the CFTR gene (study 661-106)

The mean absolute change (SE) from baseline in ppFEV₁ was 3.5 (0.6) percentage points in the Symkevi in combination with ivacaftor group and -0.4 (0.6) percentage points in the placebo group in study 661-106. Patients who received Symkevi in combination with ivacaftor in study 661-106 and continued on treatment showed sustained improvements in ppFEV₁ through 96 weeks in study 661-110 [within-group change=1.5 (1.6) percentage points]. Patients who were previously treated with placebo and received Symkevi in combination with ivacaftor in study 661-110 showed an increase of 0.9 (1.7) percentage points.

The mean absolute change (SE) from baseline in BMI z-value was -0.01(0.05) kg/m² in the Symkevi in combination with ivacaftor group and 0.00 (0.05) kg/m² in the placebo group in study 661-106. In study 661-110, the change in BMI z-value in the Symkevi in combination with ivacaftor group was maintained and patients previously treated with placebo showed an increase of 0.12 (0.07) kg/m².

Adolescent patients with CF who were heterozygous for the F508del mutation and a second mutation associated with residual CFTR activity (study 661-108)

The mean absolute change (SE) from baseline in ppFEV₁ was 11.7 (1.2) percentage points in the Symkevi in combination with ivacaftor group, 7.6 (1.2) percentage points in the ivacaftor group and -0.4 (1.2) percentage points in the placebo group in study 661-108. Patients who received Symkevi in combination with ivacaftor in study 661-108 and continued on treatment showed sustained improvements in ppFEV₁ through 96 weeks in study 661-110 [within-group change=16.9 (4.0) percentage points]. Patients who were previously treated with ivacaftor or placebo and received Symkevi in combination with ivacaftor in study 661-110 showed an increase of 4.1 (4.5) percentage points and 6.0 (3.5) percentage points, respectively.

The mean absolute change (SE) from baseline in BMI z-value was 0.24 (0.07) kg/m² in the Symkevi in combination with ivacaftor group, 0.20 (0.07) kg/m² in the ivacaftor group and 0.04 (0.07) kg/m² in the placebo group in study 661-108. In study 661-110, the change in BMI z-value were maintained in the Symkevi in combination with ivacaftor group 0.29 (0.22) kg/m², in the ivacaftor group 0.23 (0.27) kg/m², and in the placebo group 0.23 (0.19) kg/m².

Paediatric patients aged 6 to <12 years

Study 661-115

Study 661-115 was an 8-week, double-blind, phase 3 trial in 67 patients aged 6 to less than 12 years (mean age 8.6 years) who were randomised 4:1 to either Symkevi or a blinding group. The Symkevi group included patients who were homozygous for the F508del mutation (F/F) (n=42) or heterozygous for the F508del mutation and a second mutation associated with residual CFTR activity (F/RF) (n=12). Blinding groups were placebo if homozygous F/F (n=10), or ivacaftor if heterozygous F/RF (n=3). Fifty-four patients received either tezacaftor 50 mg/ivacaftor 75 mg and ivacaftor 75 mg (patients weighing < 40 kg at baseline) or tezacaftor 100 mg/ivacaftor 150 mg and ivacaftor 150 mg (patients weighing ≥ 40 kg at baseline), 12 hours apart. Patients receiving tezacaftor/ivacaftor had a screening ppFEV₁ ≥ 70% [mean baseline ppFEV₁ of 86.5% (range: 57.9, 124.1%)], baseline LCI_2.5 of 9.56 (range: 6.95, 15.52), and weight ≥ 15 kg. Patients with abnormal hepatic or renal function were excluded from the study. Abnormal hepatic impairment was defined as any two or more of ≥ 3 x ULN AST, ALT, GGT, ALP; ≥ 2 x ULN total bilirubin; or ≥ 5 x ULN ALT or AST. Abnormal renal function was defined as GFR ≤ 45 mL/min/1.73 m² calculated by the Counahan-Barratt equation.

In study 661-115, treatment with Symkevi in combination with ivacaftor resulted in a statistically significant within-group reduction from baseline in LCI_2.5 through week 8. Reduction in LCI_2.5 was observed at week 2 and was sustained through week 8. See Table 7 for a summary of primary and key secondary endpoints. Growth parameters, which were exploratory endpoints, remained stable over 8 weeks of Symkevi treatment.

In subgroup analyses of F/F and F/RF patients, the within group mean absolute change in LCI_2.5 was -0.39 (95% CI: -0.67, -0.10) and -0.92 (95% CI: -1.65, -0.20), respectively. The within group mean change in CFQ-R respiratory domain scores in F/F and F/RF patients was 1.4 points (95% CI: -1.9, 4.7) and 5.6 points (95% CI: -2.8, 13.9), respectively.

The tezacaftor 100 mg/ivacaftor 150 mg and ivacaftor 150 mg dose has not been investigated in clinical studies in children aged 6 to less than 12 years weighing 30 to < 40 kg.

Study 661-116 part A

Study 661-116 part A was a phase 3, open-label, multicentre, rollover, 96-week study to evaluate the safety and efficacy of long-term treatment with Symkevi in combination with ivacaftor in patients aged 6 years and older. Patients in study 661-116 part A rolled over from studies 661-113 part B (n=64) and 661-115 (n=66). Study 661-113 was a phase 3, open-label study to evaluate the safety and efficacy of Symkevi in combination with ivacaftor in patients 6 to less than 12 years of age. The LS mean estimates for 661-115 rollovers were calculated on patients who were randomized to the tezacaftor/ivacaftor arm in the parent study (n=53). Efficacy was a secondary objective for study part A.

The changes observed during the parent studies were maintained over 96 weeks of treatment with Symkevi in combination with ivacaftor.

At week 96, the LS mean absolute change from parent baseline in LCI_2.5 for patients from study 661-115 was -0.95 (95% CI: -1.38, -0.52).

The LS mean absolute change from parent baseline in CFQ-R respiratory domain for patients from study 661-113 part B was 6.0 points (95% CI: 1.1, 10.8), and for patients from study 661-115 was 6.4 points (95% CI: 3.5, 9.3).

The LS mean absolute change from parent baseline in BMI z-score for patients from study 661-113 part B was -0.07 (SD: 0.61), and for patients from study 661-115 was 0.05 (SD: 0.52).

Children aged less than 6 years

The European Medicines Agency has deferred the obligation to submit the results of studies with Symkevi in combination with ivacaftor in one or more subsets of the paediatric population in cystic fibrosis. See section 4.2 for information on paediatric use.

The pharmacokinetics of tezacaftor and ivacaftor are similar between healthy adult volunteers and patients with CF. Following once daily dosing of tezacaftor and twice-daily dosing of ivacaftor in patients with CF, plasma concentrations of tezacaftor and ivacaftor reach steady-state within 8 days and within 3 to 5 days, respectively, after starting treatment. At steady-state, the accumulation ratio is approximately 2.3 for tezacaftor and 3.0 for ivacaftor. Exposures of tezacaftor (administered alone or in combination with ivacaftor) increase in an approximately dose-proportional manner with increasing doses from 10 mg to 300 mg once daily. Key pharmacokinetic parameters for tezacaftor and ivacaftor at steady-state are shown in Table 8.

Absorption

After a single dose in healthy subjects in the fed state, tezacaftor was absorbed with a median (range) time to maximum concentration (t_max) of approximately 4 hours (2 to 6 hours). The median (range) t_max of ivacaftor was approximately 6 hours (3 to 10 hours) in the fed state. The AUC of tezacaftor did not change when given with fat-containing food relative to fasted conditions. The AUC of ivacaftor when given in combination with tezacaftor increased approximately 3-fold when given with fat-containing food; therefore, Symkevi and ivacaftor should be administered with fat-containing food.

Distribution

Tezacaftor is approximately 99% bound to plasma proteins, primarily to albumin. Ivacaftor is approximately 99% bound to plasma proteins, primarily to alpha 1-acid glycoprotein and albumin. After oral administration of tezacaftor 100 mg once daily in combination with ivacaftor 150 mg every 12 hours in patients with CF in the fed state, the mean (± SD) for apparent volume of distribution of tezacaftor and ivacaftor was 271 (157) L and 206 (82.9) L, respectively. Neither tezacaftor nor ivacaftor partition preferentially into human red blood cells.

Biotransformation

Tezacaftor is metabolized extensively in humans. In vitro data suggested that tezacaftor is metabolized mainly by CYP3A4 and CYP3A5. Following oral administration of a single dose of 100 mg ¹⁴C-tezacaftor to healthy male subjects, M1-TEZ, M2-TEZ, and M5-TEZ were the three major circulating metabolites of tezacaftor in humans, contributing to 15%, 31%, and 33% of total radioactivity, respectively. Under steady-state, for each of the metabolites, exposure to M1-TEZ, M2-TEZ and M5-TEZ is approximately 1.5-fold higher than for tezacaftor. M1-TEZ has similar potency to that of tezacaftor and is considered pharmacologically active. M2-TEZ is much less pharmacologically active than tezacaftor or M1-TEZ, and M5-TEZ is not considered pharmacologically active. Another minor circulating metabolite, M3-TEZ, is formed by direct glucuronidation of tezacaftor.

Ivacaftor is also metabolized extensively in humans. In vitro and in vivo data indicate that ivacaftor is metabolized primarily by CYP3A4 and CYP3A5. M1-IVA and M6-IVA are the two major metabolites of ivacaftor in humans. M1-IVA has approximately one-sixth the potency of ivacaftor and is considered pharmacologically active. M6-IVA is not considered pharmacologically active.

The effect of the CYP3A4*22 heterozygous genotype on tezacaftor and ivacaftor exposure is consistent with the effect of co-administration of a weak CYP3A4 inhibitor, which is not clinically relevant. No dose-adjustment of tezacaftor and ivacaftor is considered necessary. No data are available for CYP3A4*22 homozygous genotype patients.

Elimination

After oral administration of tezacaftor 100 mg once daily in combination with ivacaftor 150 mg every 12 hours in patients with CF in the fed state, the mean (± SD) for apparent clearance values of tezacaftor and ivacaftor were 1.31 (0.41) and 15.7 (6.38) L/h, respectively. After steady-state dosing of tezacaftor in combination with ivacaftor in CF patients, the mean (SD) terminal half-lives of tezacaftor and ivacaftor were approximately 156 (52.7) and 9.3 (1.7) hours, respectively. The mean (SD) elimination half-lives for M1-TEZ, M2-TEZ and M5-TEZ were similar to that of the parent compound. The mean (SD) elimination half-lives for M1-IVA and M6-IVA were 11.3 (2.12) h and 14.4 (6.14) h, respectively.

Following oral administration of ¹⁴C-tezacaftor, the majority of the dose (72%) was excreted in the faeces (unchanged or as the M2-TEZ metabolite) and about 14% was recovered in urine (mostly as M2-TEZ metabolite), resulting in a mean overall recovery of 86% up to 21 days after the dose. Less than 1% of the administered dose was excreted in urine as unchanged tezacaftor, showing that renal excretion is not the major pathway of tezacaftor elimination in humans.

Following oral administration of ivacaftor alone, the majority of ivacaftor (87.8%) is eliminated in the faeces after metabolic conversion. There was negligible urinary excretion of ivacaftor as unchanged medicine.

Hepatic impairment

Following multiple doses of tezacaftor and ivacaftor for 10 days, subjects with moderately impaired hepatic function (Child-Pugh Class B, score 7 to 9) had an approximately 36% increase in AUC and a 10% increase in C_max for tezacaftor, and a 50% increase in ivacaftor AUC compared with healthy subjects matched for demographics. Based on these results, a modified regimen of Symkevi is recommended for patients with moderate hepatic impairment (see Table 3 in section 4.2).

The impact of severe hepatic impairment (Child-Pugh Class C, score 10 to 15) on the pharmacokinetics of tezacaftor and ivacaftor has not been studied. The magnitude of increase in exposure in these patients is unknown but is expected to be higher than that observed in patients with moderate hepatic impairment. The use of Symkevi in patients with severe hepatic impairment is therefore not recommended unless the benefits outweigh the risks (see Table 3 in section 4.2).

No dose adjustment is considered necessary for patients with mild hepatic impairment.

Renal impairment

Tezacaftor alone or in combination with ivacaftor has not been studied in patients with moderate or severe renal impairment (creatinine clearance ≤ 30 mL/min) or in patients with end-stage renal disease. In a human pharmacokinetic study with tezacaftor alone, there was minimal elimination of tezacaftor and its metabolites in urine (only 13.7% of total radioactivity was recovered in the urine with 0.79% as unchanged medicinal product).

In a human pharmacokinetic study with ivacaftor alone, there was minimal elimination of ivacaftor and its metabolites in urine (only 6.6% of total radioactivity was recovered in the urine).

In population pharmacokinetic analysis, data from 665 patients on tezacaftor or tezacaftor in combination with ivacaftor in phase 2/3 clinical studies indicated that mild renal impairment [N=147; estimated glomerular filtration rate (eGFR), estimated by the modification of diet in renal disease method, 60 to ≤ 89 mL/min/1.73 m²] and moderate renal impairment (N=7; eGFR 30 to < 60 mL/min/1.73 m²) did not affect the clearance of tezacaftor significantly. No dose adjustment is recommended for mild and moderate renal impairment. Caution is recommended when administering Symkevi in combination with ivacaftor to patients with severe renal impairment or end-stage renal disease.

Gender

The pharmacokinetic parameters of tezacaftor and ivacaftor are similar in males and females.

Race

Very limited pharmacokinetic data indicate comparable exposure to tezacaftor in white (n=652) and non-white (n=8) patients. Race had no clinically meaningful effect on the PK of ivacaftor in white (n=379) and non-white (n=29) patients based on a population PK analysis.

Elderly

Clinical studies of Symkevi in combination with ivacaftor did not include patients over 75 years of age. The pharmacokinetic parameters of tezacaftor in combination with ivacaftor in the elderly patients (aged 65 to 72 years) are comparable to those in younger adults.

Paediatric population

The pharmacokinetic parameters of tezacaftor and ivacaftor are presented in Table 9. The pharmacokinetics of tezacaftor/ivacaftor in children below 6 years of age has not been investigated.

Tezacaftor

Non-clinical data reveal no special hazard for humans based on conventional studies of safety pharmacology, repeated dose toxicity, genotoxicity, carcinogenic potential, and toxicity to reproduction and development. Placental transfer of tezacaftor was observed in pregnant rats.

Juvenile toxicity studies in rats exposed during postnatal day 7 to 35 (PND 7-35) showed mortality and moribundity, even at low doses. Findings were dose-related and generally more severe when dosing with tezacaftor was initiated earlier in the postnatal period. Exposure in rats from PND 21-49 did not show toxicity at the highest dose, which was approximately two times the intended human exposure. Tezacaftor and its metabolite, M1-TEZ, are substrates for P-gp. Lower brain levels of P-gp activity in younger rats resulted in higher brain levels of tezacaftor and M1-TEZ. These findings are not relevant for the indicated paediatric population 6 to 11 years of age, for whom levels of P-gp activity are equivalent to levels observed in adults.

Ivacaftor

Non-clinical data reveal no special hazard for humans based on conventional studies of safety pharmacology, repeated dose toxicity, genotoxicity, and carcinogenic potential.

Ivacaftor was associated with slight decreases of the seminal vesicle weights, a decrease of overall fertility index and number of pregnancies in females mated with treated males and significant reductions in number of corpora lutea and implantation sites with subsequent reductions in the average litter size and average number of viable embryos per litter in treated females. The No Observed Adverse Effect Level (NOAEL) for fertility findings provides an exposure level of approximately 5 times the systemic exposure of ivacaftor and its metabolites when administered as tezacaftor/ivacaftor in adult humans at the maximum recommended human dose (MRHD).

In the pre- and post-natal study ivacaftor decreased survival and lactation indices and caused a reduction in pup body weights. The NOAEL for viability and growth in the offspring provides an exposure level of approximately 4 times the systemic exposure of ivacaftor and its metabolites when administered as tezacaftor/ivacaftor in adult humans at the MRHD. Placental transfer of ivacaftor was observed in pregnant rats and rabbits.

Findings of cataracts were observed in juvenile rats dosed from postnatal day 7 to 35 at ivacaftor exposure levels of 0.25 times the MRHD based on systemic exposure of ivacaftor and its metabolites when administered as tezacaftor/ivacaftor. This finding has not been observed in fetuses derived from rat dams treated with ivacaftor on gestation days 7 to 17, in rat pups exposed to ivacaftor through milk ingestion up to postnatal day 20, in 7-week-old rats, nor in 3.5- to 5-month-old dogs treated with ivacaftor. The potential relevance of these findings in humans is unknown.

Tezacaftor/ivacaftor

Combination repeat-dose toxicity studies in rats and dogs involving the co-administration of tezacaftor and ivacaftor to assess the potential for additive and/or synergistic toxicity did not produce any unexpected toxicities or interactions.

Tablet core

Hypromellose acetate succinate

Sodium laurilsulfate (E487)

Hypromellose 2910 (E464)

Microcrystalline cellulose (E460(i))

Croscarmellose sodium (E468)

Magnesium stearate (E470b)

Tablet film coat (Symkevi 50 mg/75 mg film-coated tablets)

Hypromellose 2910 (E464)

Hydroxypropyl cellulose (E463)

Titanium dioxide (E171)

Talc (E553b)

Not applicable.

3 years

This medicinal product does not require any special storage conditions.

Blister consisting of PCTFE (polychlorotrifluoroethylene)/PVC (polyvinyl chloride) with a paper-backed aluminum foil lidding.

Pack size of 28 tablets (4 blister cards of 7 tablets each).

Any unused medicinal product or waste material should be disposed of in accordance with local requirements.