AYVAKYT 25 mg film-coated tablets

Advanced systemic mastocytosis (AdvSM)

AYVAKYT is indicated as monotherapy for the treatment of adult patients with aggressive systemic mastocytosis (ASM), systemic mastocytosis with an associated haematological neoplasm (SM-AHN), or mast cell leukaemia (MCL).

Therapy should be initiated by a physician experienced in the administration of anticancer therapy.

Posology for AdvSM

The recommended starting dose of avapritinib is 200 mg orally once daily, on an empty stomach (see Method of administration). This once daily 200 mg dose is also the maximum recommended dose. Continue treatment until SM disease progression or unacceptable toxicity.

Treatment with avapritinib is not recommended in patients with a platelet count of less than 50 x 10⁹/L (see Table 2 and section 4.4).

Concomitant use of avapritinib with strong or moderate CYP3A inhibitors should be avoided. If concomitant use with a moderate CYP3A inhibitor cannot be avoided, the starting dose of avapritinib must be reduced from 200 mg to 50 mg orally once daily (see section 4.5).

Dose modifications for adverse reactions

Interruption of treatment with or without dose reduction may be considered to manage adverse reactions based on severity and clinical presentation.

The dose should be adjusted based on safety and tolerability.

The recommended dose reductions and modifications for adverse reactions are provided in Tables 1 and 2.

Table 1. Recommended dose reductions for AYVAKYT for adverse reactions

Table 2. Recommended dose modifications for AYVAKYT for adverse reactions

* The severity of adverse reactions graded by the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 4.03 and 5.0

** Adverse reactions with impact on Activities of Daily Living (ADLs) for Grade 2 or higher adverse reactions

Missed doses

If a dose of avapritinib is missed, the patient should make up for the missed dose unless the next scheduled dose is within 8 hours (see Method of administration). If the dose has not been taken at least 8 hours prior to the next dose, then that dose should be omitted and the patient should resume treatment with the next scheduled dose.

If vomiting occurs after taking a dose of avapritinib, the patient should not take an additional dose but continue with the next scheduled dose.

Special populations

Elderly

No dose adjustment is recommended for patients aged 65 years and above (see section 5.2).

Hepatic impairment

No dose adjustment is recommended for patients with mild hepatic impairment (total bilirubin within upper limit of normal [ULN] and aspartate aminotransferase (AST) > ULN or total bilirubin greater than 1 to 1.5 times ULN and any AST) and moderate hepatic impairment (total bilirubin >1.5 to 3.0 times ULN and any AST). A modified starting dose of avapritinib is recommended for patients with severe hepatic impairment (Child-Pugh Class C). The starting dose of avapritinib should be reduced from 200 mg to 100 mg orally once daily for patients with AdvSM (see section 5.2).

Renal impairment

No dose adjustment is recommended for patients with mild and moderate renal impairment [creatinine clearance (CLcr) 30-89 mL/min estimated by Cockcroft-Gault]. Avapritinib has not been studied in patients with severe renal impairment (CLcr 15-29 mL/min) or end-stage renal disease (CLcr <15 mL/min), therefore its use in patients with severe renal impairment or end-stage renal disease cannot be recommended (see section 5.2).

Paediatric population

The safety and efficacy of AYVAKYT in children aged 0 to 18 years have not yet been established. No data are available.

Method of administration

AYVAKYT is for oral use.

The tablets should be taken on an empty stomach at least 1 hour before or at least 2 hours after a meal (see section 5.2).

Patients should swallow the tablet(s) whole with a glass of water.

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

Haemorrhages

Avapritinib has been associated with an increased incidence of haemorrhagic adverse reactions, including serious and severe adverse reactions, like gastrointestinal haemorrhage and intracranial haemorrhage in patients with AdvSM (see section 4.8).

Routine surveillance of haemorrhagic events should include physical examination, and blood counts and coagulation parameters should be monitored, particularly in patients with conditions predisposing to bleeding, and in those treated with anticoagulants (e.g. warfarin, phenprocoumon, rivaroxaban, dabigatran, apixaban and edoxaban) or other concomitant medicinal products that increase the risk of bleeding (including antiplatelet therapy).

Intracranial haemorrhages

Serious adverse reactions of intracranial haemorrhage were reported in patients with AdvSM receiving avapritinib (see section 4.8). Fatal events have occurred in <1% of patients across all doses. The exact mechanism is unknown.

Before initiating avapritinib the risk for intracranial haemorrhage should be carefully considered in patients with risk factors such as severe thrombocytopenia, vascular aneurysm or a history of intracranial haemorrhage within the prior year, a history of a cerebrovascular accident or transient ischaemic attack.

Patients who experience clinically relevant neurological signs and symptoms (e.g. severe headache, vision problems, somnolence, or focal weakness) during treatment with avapritinib should interrupt treatment and inform their healthcare professional immediately. Brain imaging by magnetic resonance imaging (MRI) or computed tomography (CT) may be performed at the discretion of the physician based on severity and the clinical presentation.

For patients with observed intracranial haemorrhage during treatment with avapritinib, regardless of severity grade, avapritinib should be permanently discontinued (see section 4.2).

The incidence of intracranial haemorrhage was higher in patients with platelet counts <50 x 10⁹/L and in patients with a starting dose of ≥ 300 mg.

Considering the above, a platelet count must be performed prior to initiating therapy. Avapritinib is not recommended in patients with platelet counts <50 x 10⁹/L. Following treatment initiation, platelet counts must be performed every 2 weeks for the first 8 weeks regardless of baseline platelet count. After 8 weeks of treatment, monitor platelet counts every 2 weeks (or more frequently as clinically indicated) if values are less than 75 x 10⁹/L, every 4 weeks if values are between 75 and 100 x 10⁹/L, and as clinically indicated if values are greater than 100 x 10⁹/L.

Manage platelet counts of <50 x 10⁹/L by temporarily interrupting avapritinib. Platelet support may be necessary, and the recommended dose modification in Table 2 must be followed (see section 4.2). Thrombocytopenia was generally reversible by reducing or interrupting avapritinib in clinical studies. The maximum dose for patients with AdvSM must not exceed 200 mg once daily.

Cognitive effects

Cognitive effects can occur in patients with AdvSM receiving avapritinib (see section 4.8). These include, but are not limited to, memory impairment, cognitive disorder, confusional state, and encephalopathy. The mechanism of the cognitive effects is not known.

It is recommended that patients are clinically monitored for signs and symptoms of cognitive events such as new or increased forgetfulness, confusion, or difficulty with cognitive functioning. Patients should notify their healthcare professional immediately if they experience new or worsening cognitive symptoms.

For patients with observed cognitive effects related to treatment with avapritinib, the recommended dose modification in Table 2 should be followed (see section 4.2). In clinical studies, dose reductions or interruptions improved Grade ≥ 2 cognitive effects compared to no action.

Fluid retention

Occurrences of fluid retention, including severe cases of localised oedema (facial, periorbital, peripheral oedema and/or pleural effusion), generalised oedemas and ascites, have been reported with a frequency category of at least common in patients with AdvSM taking avapritinib. Other localised oedemas (laryngeal oedema and/or pericardial effusion) have been reported uncommonly (see section 4.8).

Therefore, it is recommended that patients be evaluated for these adverse reactions including regular assessment of weight and respiratory symptoms. An unexpected rapid weight gain or respiratory symptoms indicating fluid retention should be carefully investigated and appropriate supportive care and therapeutic measures, such as diuretics, should be undertaken. For patients presenting with ascites, it is recommended to evaluate the aetiology of ascites.

QT interval prolongation

Prolongation of QT interval has been observed in patients with AdvSM treated with avapritinib in clinical studies (see section 4.8). QT interval prolongation may induce an increased risk of ventricular arrhythmias, including Torsade de pointes.

Avapritinib should be used with caution in patients with known QT interval prolongation or at risk of QT interval prolongation (e.g. due to concomitant medicinal products that can prolong QT interval such as amiodarone, citalopram, escitalopram, ondansetron; pre-existing cardiac disease; and/or electrolyte disturbances). Concomitant administration with strong or moderate CYP3A inhibitors should be avoided due to the increased risk of adverse reactions, including QT prolongation and related arrhythmias (see section 4.5). If concomitant use of moderate CYP3A inhibitors cannot be avoided, see section 4.2 for dose modification instructions.

Interval assessments of QT by electrocardiogram (ECG) should be considered if avapritinib is taken concurrently with medicinal products that can prolong QT interval.

Gastrointestinal disorders

Diarrhoea, nausea and vomiting were the most commonly reported gastrointestinal adverse reactions in patients with AdvSM (see section 4.8). Patients who present with diarrhoea, nausea and vomiting should be evaluated to exclude disease-related aetiologies. Supportive care for gastrointestinal adverse reactions requiring treatment may include medicinal products with antiemetic, antidiarrheal, or antacid properties.

The hydration status of patients experiencing gastrointestinal adverse reactions must be closely monitored and treated as per standard clinical practice.

Laboratory tests

Treatment with avapritinib in patients with AdvSM is associated with anaemia, neutropenia and/or thrombocytopenia (see section 4.8). Complete blood counts should be performed on a regular basis during the treatment with avapritinib in patients with AdvSM (see also the guidance under intracranial haemorrhages above in this section).

Treatment with avapritinib is associated in patients with AdvSM with elevations in bilirubin and liver transaminases (see section 4.8). Liver function (transaminases bilirubin) should be monitored regularly in patients receiving avapritinib.

CYP3A4 inhibitors and inducers

Co-administration with strong or moderate CYP3A inhibitors should be avoided because it may increase the plasma concentration of avapritinib (see sections 4.2 and 4.5).

Co-administration with strong or moderate CYP3A inducers should be avoided because it may decrease the plasma concentrations of avapritinib (see section 4.5).

Photosensitivity reaction

Exposure to direct sunlight should be avoided or minimised due to the risk of phototoxicity associated with avapritinib. Patients should be instructed to use measures such as protective clothing and sunscreen with high sun protection factor (SPF).

Sodium

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

Active substances that may have an effect on avapritinib

Strong and moderate CYP3A inhibitors

Co-administration of avapritinib with a strong CYP3A inhibitor increased avapritinib plasma concentrations and may result in increased adverse reactions. Co-administration of itraconazole (200 mg twice daily on Day 1 followed by 200 mg once daily for 13 days) with a single 200 mg dose of avapritinib on Day 4 in healthy subjects increased avapritinib C_max by 1.4-fold and AUC_0-inf by 4.2-fold, relative to a 200 mg dose of avapritinib administered alone.

Concomitant use of avapritinib with strong or moderate CYP3A inhibitors (such as antifungals including ketoconazole, itraconazole, posaconazole, voriconazole; certain macrolides such as erythromycin, clarithromycin and telithromycin; active substances to treat human immunodeficiency virus infections/acquired immunodeficiency syndrome (HIV/AIDS) such as cobicistat, indinavir, lopinavir, nelfinavir, ritonavir and saquinavir; as well as conivaptan for hyponatremia and boceprevir to treat hepatitis) including grapefruit or grapefruit juice should be avoided. If concomitant use with a moderate CYP3A inhibitor cannot be avoided, the starting dose of avapritinib should be reduced from 200 mg to 50 mg orally once daily for patients with AdvSM (see section 4.2 and 4.4).

Strong and moderate CYP3A inducers

Co-administration of avapritinib with a strong CYP3A inducer decreased avapritinib plasma concentrations and may result in decreased efficacy of avapritinib. Co-administration of rifampicin (600 mg once daily for 18 days) with a single 400 mg dose of avapritinib on Day 9 in healthy subjects decreased avapritinib C_max by 74% and AUC_0-inf by 92%, relative to a 400 mg dose of avapritinib administered alone.

Co-administration of avapritinib with strong and moderate CYP3A inducers (e.g. dexamethasone, phenytoin, carbamazepine, rifampicin, phenobarbital, fosphenytoin, primidone, bosentan, efavirenz, etravirine, modafinil, dabrafenib, nafcillin or Hypericum perforatum, also known as St. John's wort) should be avoided.

Effect of avapritinib on other active substances

In vitro studies demonstrated that avapritinib is a direct inhibitor of CYP3A and a time-dependent inhibitor of CYP3A. Therefore, avapritinib may have the potential to increase plasma concentrations of co-administered medicinal products that are substrates of CYP3A.

In vitro studies indicated that avapritinib is an inducer of CYP3A. Therefore, avapritinib may have the potential to decrease plasma concentrations of co-administered medicinal products that are substrates of CYP3A.

Caution should be exercised with co-administration of avapritinib with narrow therapeutic index CYP3A substrates (e.g. alfentanil, ciclosporin, dihydroergotamine, ergotamine, fentanyl, pimozide, sirolimus, tacrolimus) and with medicinal products that can increase the risk of QT prolongation (e.g. amiodarone, citalopram, escitalopram, ondansetron) as their plasma concentrations may be altered.

Avapritinib is an inhibitor of P-gp, BCRP, MATE1, MATE2-K, and BSEP in vitro. Therefore, avapritinib has the potential to alter concentrations of co-administered substrates of these transporters.

Women of childbearing potential/Contraception in males and females

Women of childbearing potential should be informed that avapritinib may cause foetal harm (see section 5.3).

The pregnancy status of women of reproductive potential should be verified prior to initiating avapritinib treatment.

Women of childbearing potential should use effective contraception during treatment and for 6 weeks after the last dose of avapritinib. Males with female partners of childbearing potential must use effective contraception during treatment and for 2 weeks after the last dose of avapritinib.

Patients should be advised to contact their healthcare professional immediately if they become pregnant, or if pregnancy is suspected, while taking avapritinib.

Pregnancy

There are no data from the use of avapritinib in pregnant women. Studies in animals have shown reproductive toxicity (see section 5.3).

Avapritinib is not recommended during pregnancy and in women of childbearing potential not using contraception.

If avapritinib is used during pregnancy or if the patient becomes pregnant while taking avapritinib, the patient should be advised of the potential risk to the foetus.

Breast-feeding

It is unknown whether avapritinib/ metabolites are excreted in human milk.

A risk to the newborns/infants cannot be excluded.

Breast-feeding should be discontinued during treatment with avapritinib and for 2 weeks following the final dose.

Fertility

There are no data on the effect of avapritinib on human fertility. No relevant effects on fertility were observed in a rat fertility study (see section 5.3).

Avapritinib may cause adverse reactions such as cognitive effects that may influence the ability to drive and use machines.

Patients should be made aware of the potential for adverse reactions that affect their ability to concentrate and react. Patients who experience these adverse effects should take special care when driving a car or operating machinery.

Summary of the safety profile

The safety database includes a total of 193 patients enrolled in studies for AdvSM (all doses), of which 126 patients received avapritinib at a starting dose of 200 mg, see section 5.1.

The most common adverse reactions of any grade during treatment with avapritinib at a starting dose of 200 mg were periorbital oedema (38%), thrombocytopenia (37%), oedema peripheral (33%), and anaemia (22%).

Serious adverse reactions occurred in 12% of patients receiving avapritinib. The most common serious adverse reactions during treatment with avapritinib were subdural haematoma (2%), anaemia (2%), and haemorrhage (2%).

In AdvSM patients treated at 200 mg, 7.1% had adverse reactions leading to permanent treatment discontinuation. In two patients (1.6%), subdural haematoma occurred. Cognitive disorder, depressed mood, diarrhoea, disturbance in attention, haemoglobin decreased, hair colour changes, libido decreased, nausea, neutropenia, premature menopause and thrombocytopenia occurred in one patient (0.8% each). Adverse reactions leading to a dose reduction included thrombocytopenia, neutropenia, periorbital oedema, cognitive disorder, oedema peripheral, platelet count decreased, neutrophil count decreased, anaemia, asthenia, fatigue, arthralgia, blood alkaline phosphatase increased, blood bilirubin increased, and white blood cell count decreased.

Tabulated list of adverse reactions

For patients with AdvSM, adverse reactions that were reported in clinical studies in ≥ 3% of patients are listed below (Table 3) except for adverse reactions mentioned in the section 4.4 which are included regardless of frequency, according to the MedDRA System Organ Class and frequency.

Frequencies are defined using the following convention: 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).

Within each frequency grouping, adverse reactions are presented in order of decreasing seriousness.

Table 3. Adverse reactions reported in clinical studies in patients with advanced systemic mastocytosis treated with avapritinib starting at 200 mg

¹Cognitive effects (including cognitive disorder, memory impairment and confusional state)

²Neuropathy peripheral (including Paraesthesia, Neuropathy peripheral, Hypoaesthesia)

³Intracranial haemorrhage (including Haemorrhage intracranial, Subdural haematoma)

⁴Gastrointestinal haemorrhage (including Gastric haemorrhage, Gastrointestinal haemorrhage, Melaena)

⁵Oedema (including Periorbital oedema, Oedema peripheral, Face oedema, Eyelid oedema, Fluid retention, Generalised oedema, Oedema, Peripheral swelling, Swelling face, Eye swelling, Conjunctival oedema, Laryngeal oedema, Localised oedema)

^*Comprises pooled terms representing similar medical concepts.

-: no adverse reactions reported

Description of selected adverse reactions

Intracranial haemorrhage

Fatal events of intracranial haemorrhage have occurred in less than 1% of patients with AdvSM (all doses).

Intracranial haemorrhage occurred in a total (regardless of causality) of 4 (3.2%) of the 126 patients with AdvSM who received avapritinib at a starting dose of 200 mg once daily regardless of platelet count prior to initiation of therapy. In 3 of these 4 patients, the event was assessed as related to avapritinib (2.4%). The risk of intracranial haemorrhagic events is higher in patients with platelet counts <50 x 10⁹/L. Intracranial haemorrhage occurred in 2.5% of the 121 patients with AdvSM with platelet counts of ≥ 50 x 10⁹/L prior to initiation of therapy who received avapritinib at the recommended starting dose of 200 mg.

Events of intracranial haemorrhage (all grades) occurred in a range from 12.0 weeks to 15.0 weeks after initiating avapritinib, with a median time to onset of 12.1 weeks.

In clinical studies with avapritinib, the incidence of intracranial haemorrhage was higher in patients who received a starting dose of ≥ 300 mg once daily, as compared to patients who received the recommended starting dose of 200 mg once daily. The maximum dose for patients with AdvSM must not exceed 200 mg once daily.

Cognitive effects

A broad spectrum of cognitive effects that are generally reversible (with intervention) can occur in patients receiving avapritinib. Cognitive effects were managed with dose interruption and/or reduction, and 2.7% led to permanent discontinuation of avapritinib treatment.

Cognitive effects occurred in 51 (26%) of the 193 patients with AdvSM (all doses) and in 23 (18%) of the 126 patients with AdvSM who received avapritinib at a starting dose of 200 mg (see section 4.4). In the patients with AdvSM treated at a starting dose of 200 mg who had an event (any grade), the median time to onset was 12 weeks (range: 0.1 weeks to 108.1 weeks).

Most cognitive effects were Grade 1, with Grade ≥ 2 occurring in 7% of 126 patients treated at a starting dose of 200 mg. Among patients who experienced a cognitive effect of Grade ≥ 2 (impacting activities of daily living) the median time to improvement was 6 weeks.

For patients with AdvSM treated at a starting dose of 200 mg cognitive disorder occurred in 12% of patients; 1.6% of these events were Grade 3. Memory impairment occurred in 6% of patients; none of these events were Grade 3. Confusional state occurred in 2% of patients; none of these events were Grade 3. No Grade 4 and no fatal events were reported.

Of the 126 AdvSM patients treated at a starting dose of 200 mg one patient (<1%) required permanent discontinuation of avapritinib for a cognitive adverse reaction, 7% required a dose interruption, and 6% required dose reduction.

Cognitive effects occurred in 20% of the patients aged ≥ 65 years receiving a starting dose of 200 mg once daily.

Elderly

Of the 126 patients with AdvSM who received avapritinib at a starting dose of 200 mg once daily in EXPLORER and in PATHFINDER, 63% were 65 years or older and 21% were 75 years of age or older. Compared with younger patients (<65), more patients ≥ 65 years old reported adverse reactions that led to dose reductions (62% versus 73%). A similar fraction of patients reported adverse reactions that led to dose discontinuation (9% versus 6%). The types of adverse reactions reported were similar regardless of age. Older patients reported more Grade 3 or higher adverse reactions (63.3%) compared to younger patients (53.2%).

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

Symptoms

There is limited experience with cases of overdose reported in clinical studies with avapritinib. The maximum dose of avapritinib studied clinically is 600 mg orally once daily. Adverse reactions observed at this dose were consistent with the safety profile at the recommended dose (see section 4.8).

Management

There is no known antidote for avapritinib overdose. In the event of suspected overdose, avapritinib should be interrupted and supportive care instituted. Based on the large volume of distribution of avapritinib and extensive protein binding, dialysis is unlikely to result in significant removal of avapritinib.

Pharmacotherapeutic group: antineoplastic agents, protein kinase inhibitor, ATC code: L01EX18.

Mechanism of action

Avapritinib is a Type 1 kinase inhibitor that has demonstrated biochemical in vitro activity on the PDGFRA D842V and KIT D816V mutants associated with resistance to imatinib, sunitinib and regorafenib with half maximal inhibitory concentrations (IC₅₀) of 0.24 nM and 0.27 nM, respectively, and greater potency against clinically relevant KIT exon 11, KIT exon 11/17 and KIT exon 17 mutants than against the KIT wild-type enzyme.

In cellular assays avapritinib inhibited the proliferation in KIT mutant cell lines, including a murine mastocytoma cell line and a human mast cell leukaemia cell line. Avapritinib also showed growth inhibitory activity in a xenograft model of murine mastocytoma with KIT exon 17 mutations.

Pharmacodynamic effects

Potential to prolong the QT interval

The ability of avapritinib to prolong the QT interval was assessed in 27 patients administered avapritinib at doses of 300/400 mg once daily in an open-label, single-arm study in patients with GIST. The estimated mean change from baseline in QTcF was 6.55 ms (90% confidence interval [CI]: 1.80 to 11.29) at the observed steady state geometric mean C_max of 899 ng/mL. No effect on heart rate or cardiac conduction (PR, QRS, and RR intervals) was observed.

Clinical efficacy and safety

The efficacy and safety of avapritinib was assessed in BLU-285-2202 (PATHFINDER), a multi-centre, single-arm, open-label Phase 2 clinical study. Eligible patients were required to have an ECOG PS of 0 to 3. Patients with high and very high risk AHNs such as AML or high risk MDS, and Philadelphia chromosome-positive malignancies were excluded. Palliative and supportive care medications were allowed. Response-evaluable patients included those with a confirmed diagnosis of AdvSM per the World Health Organisation (WHO) and deemed evaluable by modified IWG-MRT-ECNM criteria at baseline as adjudicated by an independent central committee, who received at least 1 dose of avapritinib, had at least 2 post-baseline bone marrow assessments and had been on study for at least 24 weeks, or had an end of study visit.

In PATHFINDER, patients were enrolled at the starting dose of 200 mg orally once daily. The primary efficacy outcome measure was ORR according to modified IWG-MRT-ECNM criteria as evaluated by the central committee in 72 patients treated with avapritinib starting dose of 200 mg daily. Additional efficacy outcome measures were duration of response (DOR), time to response, overall survival (OS) and changes in individual measures of mast cell burden.

The assessment of the primary efficacy endpoint, the ORR, was based on a total of 72 patients with AdvSM, enrolled in PATHFINDER, who were evaluable for response. The median duration of follow up for these patients was 14.3 months (95% confidence interval 11.2 to 16.9 months).

The study population characteristics were: median age of 68 years (range: 31 to 88 years), 58% male, 85% white, 75% had an ECOG PS of 0-1, 25% had an ECOG PS of 2-3, 33% had ongoing corticosteroid therapy use for systemic mastocytosis at baseline, 90% of patients had a detectable KIT D816V mutation, 64% had prior antineoplastic therapy and 53% had received prior midostaurin. Before initiation of avapritinib treatment, the median bone marrow mast cell infiltrate was 50%, the median serum tryptase level was 259.20 ng/mL, and the median KIT D816V mutant allele fraction (MAF) was 15%.

Efficacy results in patients with AdvSM enrolled in the PATHFINDER study, who were treated with a starting dose of 200 mg once daily is summarized in Table 4.

Table 4. Efficacy results for patients with advanced systemic mastocytosis in PATHFINDER per modified IWG-MRT-ECNM criteria

Abbreviations: CI=confidence interval; CR=complete response; CRh = complete remission with partial recovery of peripheral blood counts; DOR=duration of response; NE=not estimable; ORR=overall response rate; PR=partial response

^a ORR is defined as patients who achieved a CR, CRh, PR or clinical improvement

^b DOR is defined as duration of response for patients who achieve a CR, CRh, PR or clinical improvement, DOR is estimated from Kaplan-Meyer analysis

The assessment of the following secondary efficacy endpoints was based on AdvSM patients with baseline and post baseline values for mast cell burden. 83.5% of patients had a decrease in bone marrow infiltration that exceeded 50% with 60.2% patients having complete elimination of bone marrow mast cell aggregates; 90.5% had a decrease in serum tryptase levels that exceeded 50%, with 53.3% reducing serum tryptase <20 ng/mL; and 76.2% of patients had a decrease in KIT D816V variant allele fraction in blood that exceeded 50% with decrease to <1% in 45.7% of patients and 62.1% of patients had a reduction of ≥ 35% in spleen volume, which correlates with a 50% decrease by palpation.

Among the 35 patients receiving 200 mg orally daily with baseline corticosteroid use in the AdvSM population, 51% of patients reduced their corticosteroid use or discontinued corticosteroids completely.

SM symptoms were a secondary endpoint in the PATHFINDER study and were measured using the AdvSM-Symptom Assessment Form (AdvSM-SAF) questionnaire. The AdvSM-SAF is a 10-item questionnaire to assess 8 symptoms (abdominal pain, nausea, vomiting, diarrhoea, spots on skin, itching, flushing, fatigue) and 2 functional domains (GI and skin) specific to AdvSM. Total symptom score (TSS) is the sum of all 8 symptoms (scored 0 to 80). The assessment of the following secondary efficacy endpoints was based on AdvSM patients with a baseline value for the respected symptom/domain/TSS. In patients on treatment for > 10 cycles, mean change in AdvSM-SAF TSS from baseline to C11D1 was statistically significant (p value< 0.001). The mean reduction from baseline was − 6.70 points (95% confidence interval: − 9.30 to − 4.11).

In a supportive multi-center, single-arm, open-label Phase 1 study BLU-285-2101 (EXPLORER), the ORR according to the mIWG-MRT-ECNM criteria was 68.8% (95% confidence interval: 41.3, 89.0) for 16 AdvSM patients who received a starting dose of 200 mg avapritinib once daily.

Elderly population

Of the 126 patients with AdvSM who received avapritinib at a starting dose of 200 mg once daily in EXPLORER and in PATHFINDER 63% were 65 years or older. No overall differences in efficacy were observed in comparison with younger patients.

Paediatric population

The Medicines and Healthcare products Regulatory Agency (MHRA) has waived the obligation to submit the results of studies with AYVAKYT in all subsets of the paediatric population with mastocytosis (see section 4.2 for information on paediatric use).

This medicinal product has been authorised under a so-called 'conditional approval' scheme.

This means that further evidence on this medicinal product is awaited.

The Medicines and Healthcare products Regulatory Agency (MHRA) will review new information on this medicinal product at least every year and this SmPC will be updated as necessary.

Following administration of avapritinib once daily, steady state was reached by 15 days.

Steady-state C_max and AUC of avapritinib increased proportionally over the dose range of 30 mg to 400 mg once daily in patients with AdvSM. The steady state geometric mean (CV%) C_max and AUC_0-24 of avapritinib at 200 mg once daily was 377 ng/mL (62%) and 6600 h• ng/mL (54%), respectively. The geometric mean accumulation ratio after repeat dosing was 2.6 to 5.8.

Absorption

Following administration of single oral doses of avapritinib of 30 to 400 mg, the median time to peak concentration (T_max) ranged from 2 to 4 hours post dose. The absolute bioavailability has not been determined. The population estimated mean oral bioavailability of avapritinib in patients with AdvSM is 20% lower, compared to that in the patients with GIST.

Effect of food

Avapritinib C_max and AUC_inf were increased by 59% and 29%, respectively, in healthy subjects administered avapritinib after a high fat meal (approximately 909 calories, 58 grams carbohydrate, 56 grams fat and 43 grams protein) compared to the C_max and AUC_inf after overnight fasting.

Distribution

Avapritinib is 98.8% bound to human plasma proteins in vitro and the binding is not concentration-dependent. The blood-to-plasma ratio is 0.95. Following a single 200 mg oral dose of avapritinib, the geometric mean apparent volume of distribution was 1900 L (43%) in patients with AdvSM, indicating extensive distribution into tissues from plasma.

Biotransformation

In vitro studies demonstrated that oxidative metabolism of avapritinib is predominantly mediated by CYP3A4, CYP3A5 and to a minor extent by CYP2C9. The relative contributions of CYP2C9 and CYP3A to the in vitro metabolism of avapritinib were 15.1% and 84.9%, respectively. The formation of the glucuronide M690 is catalysed mainly by UGT1A3.

Following a single dose of approximately 310 mg (~100 µ Ci) [¹⁴C]avapritinib to healthy subjects, oxidation, glucuronidation, oxidative deamination and N-dealkylation were the primary metabolic pathways. Unchanged avapritinib (49%) and metabolites, M690 (hydroxy glucuronide; 35%) and M499 (oxidative deamination; 14%) were the major circulating radioactive components. Following oral administration of avapritinib 300 mg once daily in patients, the steady state AUC of the constitutive enantiomers of M499, BLU111207 and BLU111208 are approximately 35% and 42% of the AUC of avapritinib. Compared to avapritinib (IC₅₀ = 4 nM), the enantiomers BLU111207 (IC₅₀ = 41.8 nM) and BLU111208 (IC₅₀ = 12.4 nM) are 10.5- and 3.1-fold less potent against KIT D816V in vitro.

In vitro studies demonstrated that avapritinib is a direct inhibitor of CYP3A and a time-dependent inhibitor of CYP3A4, at clinically relevant concentrations (see section 4.5). In vitro, avapritinib did not inhibit CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C19, or CYP2D6 at clinically relevant concentrations.

In vitro, at clinically relevant concentrations, avapritinib induced CYP3A (see section 4.5). In vitro, avapritinib did not induce CYP1A2 or CYP2B6 at clinically relevant concentrations.

Elimination

Following single doses of avapritinib of 30 to 400 mg in patients with AdvSM, the mean plasma elimination half-life of avapritinib was 20 to 39 hours.

Following oral administration of avapritinib 200 mg once daily, the steady state mean apparent oral clearance (CL/F) of avapritinib was 40.3 L/h in patients with AdvSM.

Following a single oral dose of approximately 310 mg (~100 µ Ci) [¹⁴C]avapritinib to healthy subjects, 70% of the radioactive dose was recovered in faeces and 18% excreted in urine. Unchanged avapritinib accounted for 11% and 0.23% of the administered radioactive dose excreted in faeces and urine, respectively.

Effects of avapritinib on transport proteins

In vitro, avapritinib is not a substrate of P-gp, BCRP, OAT1, OAT3, OCT1, OCT2, OATP1B1, OATP1B3, MATE1, MATE2-K and BSEP at clinically relevant concentrations.

Avapritinib is an inhibitor of P-gp, BCRP, MATE1, MATE2-K, and BSEP in vitro (see section 4.5). In vitro, avapritinib did not inhibit OATP1B1, OATP1B3, OAT1, OAT3, OCT1, or OCT2 at clinically relevant concentrations.

Gastric acid reducing active substances

No clinical drug-drug interaction studies have been conducted. Based on both population and noncompartmental pharmacokinetic analyses, the effect of gastric acid reducing agents on the bioavailability of avapritinib is not clinically relevant.

Special populations

Population pharmacokinetic analyses indicate that age, race, sex, body weight, and albumin concentration have no clinically meaningful effect on the pharmacokinetics of avapritinib. In clinical studies, no relevant differences in exposure, safety or efficacy were observed between elderly (aged 65 years and above) and younger patients (see also section 4.8 and section 5.1).

Hepatic impairment

As hepatic elimination is a major route of excretion for avapritinib, hepatic impairment may result in increased plasma avapritinib concentrations. Based on a population pharmacokinetic analysis, avapritinib exposures were similar between 72 subjects with mild hepatic impairment (total bilirubin within upper limit of normal [ULN] and AST > ULN or total bilirubin >1 to 1.5 times ULN and any AST), 13 subjects with moderate hepatic impairment (total bilirubin >1.5 to 3.0 times ULN and any AST), and 402 subjects with normal hepatic function (total bilirubin and AST within ULN). In a clinical study investigating the effect of severe hepatic impairment on the pharmacokinetics of avapritinib following administration of a single oral dose of 100 mg avapritinib, the mean unbound AUC was 61% higher in subjects with severe hepatic impairment (Child-Pugh Class C) as compared to matched healthy subjects with normal hepatic function. A lower starting dose is recommended in patients with severe hepatic impairment (see section 4.2).

Renal impairment

Based on a population pharmacokinetic analysis, avapritinib exposures were similar among 136 subjects with mild renal impairment (CLcr 60-89 mL/min), 52 subjects with moderate renal impairment (CLcr 30-59 mL/min) and 298 subjects with normal renal function (CLcr ≥ 90 mL/min), suggesting that no dose adjustment is necessary in patients with mild to moderate renal impairment. The pharmacokinetics of avapritinib in patients with severe renal impairment (CLcr 15-29 mL/min) or end-stage renal disease (CLcr <15 mL/min) has not been studied.

Repeat dose toxicology studies

Avapritinib was evaluated in repeat-dose toxicology studies of up to 6 months in rats and 9 months in dogs. Brain haemorrhages and hypospermatogenesis in dogs, as well as ovarian haemorrhages in rats, were not reversible with a 2-month recovery period.

Repeat dose studies in dogs indicated haemorrhage in the brain and spinal cord occurred at doses greater than or equal to 15 mg/kg/day (approximately 1.8 times the human exposure based on AUC at the 200 mg clinical dose once daily) and choroid plexus oedema in the brain occurred at doses greater than or equal to 7.5 mg/kg/day (approximately 1.0 times the human exposure based on AUC at the 200 mg clinical dose once daily). These findings were not observed in a subsequent 9-month study.

Rats manifested convulsions, which was potentially secondary to inhibition of Nav 1.2 at systemic exposures 12- -fold higher than the exposure in patients at the clinical dose of 200 mg once daily. This effect was not seen in dogs.

In a 6-month repeat dose toxicology study in rats, rats manifested haemorrhagic and cystic degeneration of the ovarian corpus lutea at 3 times the human exposure based on AUC at the 200 mg clinical dose. In a 9-month repeat dose toxicology study in dogs, minimal to mild hypospermatogenesis (3/4 males) was observed at the highest dose tested, 5 mg/kg/day (1.2 times the human exposure (AUC) at the 200 mg clinical dose).

Genotoxicity/carcinogenicity

Avapritinib was not mutagenic in vitro in the bacterial reverse mutation assay (Ames test). It was positive in the in vitro chromosome aberration test in cultured human peripheral blood lymphocytes but negative in the rat bone marrow micronucleus test, and thus, overall non-genotoxic. The carcinogenic potential of avapritinib was evaluated in a 6 month transgenic mouse study. Avapritinib was not carcinogenic up to the highest dose evaluated of 20 mg/kg/day.

Toxicity to reproduction and development

A combined male and female fertility and early embryonic development study was conducted in rats at oral avapritinib doses of 3, 10, and 30 mg/kg/day for males, and 3, 10, and 20 mg/kg/day for females. No effect on male or female fertility was noted at the highest dose levels tested in this study (approximately 8.7 times the human exposure based on AUC at the 200 mg clinical dose).

There was however an increase in pre-implantation loss and in early resorptions (approximately 3.0 times the human exposure based on AUC at the 200 mg clinical dose).

In an embryo-foetal development toxicity study in rats, avapritinib showed embryotoxic and teratogenic effects (decreases in foetal weights and viability, and increases in visceral and skeletal malformations). Oral administration of avapritinib during the period of organogenesis was teratogenic and embryotoxic in rats at exposures approximately 6.3 times the human exposure (AUC) at the 200 mg, dose.

Phototoxicity studies

An in vitro phototoxicity study in 3T3 mouse fibroblasts as well as a phototoxicity study in pigmented rats demonstrated that avapritinib has a slight potential for phototoxicity.

Tablet core

Microcrystalline cellulose

Copovidone

Croscarmellose sodium

Magnesium stearate

Tablet coat

Talc

Macrogol 3350

Poly(vinyl alcohol)

Titanium dioxide (E171)

Not applicable.

3 years

This medicinal product does not require any special storage conditions.

High-density polyethylene (HDPE) bottle with child-resistant cap (polypropylene) with foiled induction seal liner (pulp backed heat induction foil) and a desiccant in canister.

Each carton contains one bottle with 30 film-coated tablets.

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