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Trial record 2 of 7 for:    PIK3CA Related Overgrowth Spectrum

Study Assessing the Efficacy, Safety and PK of Alpelisib (BYL719) in Pediatric and Adult Patients With PIK3CA-related Overgrowth Spectrum

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04589650
Recruitment Status : Not yet recruiting
First Posted : October 19, 2020
Last Update Posted : October 19, 2020
Sponsor:
Information provided by (Responsible Party):
Novartis ( Novartis Pharmaceuticals )

Brief Summary:
This is a prospective Phase II multi-center study with an upfront 16-week, randomized, double-blind, placebo-controlled period, and extension periods, to assess the efficacy, safety and pharmacokinetics of alpelisib in pediatric and adult participants with PIK3CA-related overgrowth spectrum (PROS).

Condition or disease Intervention/treatment Phase
PIK3CA-related Overgrowth Spectrum (PROS) Drug: Alpelisib Drug: Placebo Phase 2

Expanded Access : An investigational treatment associated with this study is available outside the clinical trial.   More info ...

Detailed Description:

This study consists of a screening period of up to 42 days, core period of 24 weeks, extension period of 23 weeks and long-term extension period of up to approximately 4 years. The study will enroll adult participants (Group 1), 6-17 years old pediatric participants (Group 2), and an exploratory set of 2-5 years old pediatric participants (Group 3). At study start, only the participants of Group 1 and Group 2 will be enrolled.

Eligible participants aged ≥6 years old will be randomized in a 2:1 ratio to alpelisib or matching placebo. Both age groups will be enrolled in the study in parallel. In the core period, participants will receive treatment in blinded fashion, with an upfront 16-week placebo-controlled period. After Week 16 those participants who were randomized to receive placebo will be switched to active treatment with alpelisib. Those participants who were randomized to receive alpelisib will continue their active treatment.

Group 3 will be enrolled later, after 24-week efficacy, safety and PK data are available from the first two age groups, in order to select the recommended dose for this group.

The planned duration of alpelisib treatment in the study will be up to 5 years after randomization for all age groups. Participant may be discontinued from treatment with alpelisib earlier due to unacceptable toxicity, confirmed disease progression, death, and/or any other reason at the discretion of the investigator or the participant.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 150 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Masking Description: Participants, investigator staff, and persons performing the assessments will remain blinded to the identity of the treatment from the time of randomization until primary analysis i.e. the last participant completes Week 24 from randomization or discontinues earlier.
Primary Purpose: Treatment
Official Title: EPIK-P2: A Phase II Double-blind Study With an Upfront, 16-week Randomized, Placebo-controlled Period, to Assess the Efficacy, Safety and Pharmacokinetics of Alpelisib (BYL719) in Pediatric and Adult Patients With PIK3CA-related Overgrowth Spectrum (PROS)
Estimated Study Start Date : February 2, 2021
Estimated Primary Completion Date : January 27, 2023
Estimated Study Completion Date : December 26, 2029

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Adult cohort (group 1)- Alpelisib
During double-blind randomized study period (from baseline up to Week 16), adult participants will be randomized to receive alpelisib (125 mg, oral, once daily). After Week 16, participants will continue their active treatment at the same dose level.
Drug: Alpelisib
Adult participants (group 1) will receive 125 mg of alpelisib oral tablets once daily. Pediatric participants (Group 2: 6 to 17 years old) will receive 50 mg of alpelisib oral tablets once daily. Pediatric participants (Group 3: 2 to 5 years old) will receive alpelisib at dose determined based on the primary analysis for efficacy, safety and PK of alpelisib in Groups 1 and 2.

Placebo Comparator: Adult cohort (group 1)- Placebo
During double-blind randomized study period (from baseline up to Week 16), adult participants will be randomized to receive placebo (125 mg, oral, once daily). After Week 16, participants will be switched to active treatment with alpelisib at the placebo dose level received at the end of the placebo period.
Drug: Alpelisib
Adult participants (group 1) will receive 125 mg of alpelisib oral tablets once daily. Pediatric participants (Group 2: 6 to 17 years old) will receive 50 mg of alpelisib oral tablets once daily. Pediatric participants (Group 3: 2 to 5 years old) will receive alpelisib at dose determined based on the primary analysis for efficacy, safety and PK of alpelisib in Groups 1 and 2.

Drug: Placebo
Participants will receive matching placebo once daily up to week 16.

Experimental: Pediatric cohort (group 2: 6 to 17 years old) -Alpelisib
During double-blind randomized study period (from baseline up to Week 16, pediatric participants (6 to 17 years old) will be randomized to receive alpelisib (50 mg, oral, once daily). After Week 16, participants will continue their active treatment at the same dose level.
Drug: Alpelisib
Adult participants (group 1) will receive 125 mg of alpelisib oral tablets once daily. Pediatric participants (Group 2: 6 to 17 years old) will receive 50 mg of alpelisib oral tablets once daily. Pediatric participants (Group 3: 2 to 5 years old) will receive alpelisib at dose determined based on the primary analysis for efficacy, safety and PK of alpelisib in Groups 1 and 2.

Placebo Comparator: Pediatric cohort (group 2: 6 to 17 years old)-Placebo
During double-blind randomized study period (from baseline up to Week 16), pediatric participants (6 to 17 years old) will be randomized to receive Placebo (50mg, oral, once daily). After Week 16, participants will be switched to active treatment with alpelisib at the placebo dose level received at the end of the placebo period.
Drug: Alpelisib
Adult participants (group 1) will receive 125 mg of alpelisib oral tablets once daily. Pediatric participants (Group 2: 6 to 17 years old) will receive 50 mg of alpelisib oral tablets once daily. Pediatric participants (Group 3: 2 to 5 years old) will receive alpelisib at dose determined based on the primary analysis for efficacy, safety and PK of alpelisib in Groups 1 and 2.

Drug: Placebo
Participants will receive matching placebo once daily up to week 16.

Experimental: Pediatric cohort (group 3: 2 to 5 years old)- Alpelisib
Pediatric participants (2 to 5 years old) will receive alpelisib at dose determined based on the primary analysis for efficacy, safety and PK of alpelisib in Groups 1 and 2. An extrapolation approach will be used for dose selection for this group.
Drug: Alpelisib
Adult participants (group 1) will receive 125 mg of alpelisib oral tablets once daily. Pediatric participants (Group 2: 6 to 17 years old) will receive 50 mg of alpelisib oral tablets once daily. Pediatric participants (Group 3: 2 to 5 years old) will receive alpelisib at dose determined based on the primary analysis for efficacy, safety and PK of alpelisib in Groups 1 and 2.




Primary Outcome Measures :
  1. Proportion of participants randomized to alpelisib with a response at Week 24 in Group 1 and Group 2 [ Time Frame: Week 24 ]
    Response defined by achieving at least 20% reduction from baseline in the sum of target lesion volumes (1 to 3 lesions, assessed by MRI by a blinded independent review committee (BIRC)) at Week 24, provided that none of the individual target lesions has ≥ 20% increase from baseline and in absence of progression of non-target lesions and without new lesions.


Secondary Outcome Measures :
  1. Proportion of participants with response at Week 16 in Group 1 and Group 2 [ Time Frame: Week 16 ]
    Response defined by achieving at least 20% reduction from baseline in the sum of target lesion volumes (1 to 3 lesions, assessed by MRI by a blinded independent review committee (BIRC)) at Week 16, provided that none of the individual target lesions has ≥ 20% increase from baseline and in absence of progression of non-target lesions and without new lesions.

  2. Frequency and severity of adverse events in Group 1 and Group 2 participants with PROS over time [ Time Frame: Up to approximately 5 years ]
    Type, frequency, seriousness, and severity of treatment-emergent adverse events per CTCAE v4.03 criteria.

  3. Change from baseline to Week 16 in Brief Pain Inventory (BPI) Worst Pain intensity for alpelisib compared to placebo treatment arm in pediatric and adult populations [ Time Frame: Baseline to Week 16 ]
    The Brief Pain Inventory (BPI) item that assesses worst pain intensity in the past 24 hours will be recorded on a PRO diary. Participants respond to the item on an 11-point numerical rating scale ranging from 0 (no pain) to 10 (pain as bad as you can imagine). Change from baseline in scores at Week 16 will be assessed on treatment with alpelisib as compared to placebo in adult (≥ 18 years old) and pediatric (12 to 17 years old) populations.

  4. Change from baseline to Week 16 in Patient Global Impression of Symptom Severity (PGIS) for alpelisib compared to placebo treatment arm in pediatric and adult populations [ Time Frame: Baseline to Week 16 ]
    The PGIS is a single item to assess the participant's perception in the severity of their symptoms experienced and clinical meaningfulness of treatment effects experienced using a 5-point verbal rating scale, from "No Symptoms" to "Very Severe". Change from baseline severity at Week 16 will be assessed on treatment with alpelisib as compared to placebo in adult (≥ 18 years old) and pediatric (12 to 17 years old) populations.

  5. Duration of response (DOR) in participants who received alpelisib in Group 1 and Group 2 [ Time Frame: From first documented response until progression of PROS lesions or death, assessed up to approximately 5 years ]
    Duration of response (DOR) is defined as the time from first documented response until progression of PROS lesions by BIRC or death.

  6. Overall clinical response rate as assessed by investigator in Group 1 and Group 2 [ Time Frame: Week 16, 24, 40, 48 and thereafter every 6 months ]
    Proportion of participants with overall clinical response reported as improvement, stable or worsening of clinical condition, as assessed by the investigator

  7. Proportion of participants with response during the extension period in Group 1 and Group 2 [ Time Frame: Week 40, 48, 72, 96, 120, 144, 168, 192, 216, 240 and 264. ]
    Response (yes/no) at scheduled protocol visit. Response is defined by achieving at least 20% reduction from baseline in the sum of target lesion volumes (1 to 3 lesions, assessed by MRI by a blinded independent review committee (BIRC)), provided that none of the individual target lesions has ≥ 20% increase from baseline and in absence of progression of non-target lesions and without new lesions.

  8. Changes in symptoms and complications/comorbidities up to Week 16 on treatment with alpelisib as compared to placebo in Group 1 and Group 2 [ Time Frame: Baseline up to Week 16 ]
    Change in PROS-related symptoms and complications/comorbidities associated with PROS up to Week 16 among participants with symptoms and complications/comorbidities present at baseline

  9. Changes in symptoms and complications/comorbidities associated with PROS over time in Group 1 and Group 2 [ Time Frame: Baseline up to approximately 5 years ]
    Change in PROS-related symptoms and complications/comorbidities among participants with symptoms and complications/comorbidities present at baseline

  10. Percentage change from baseline in target and MRI-measurable non- target lesion volume in Group 1 and Group 2 [ Time Frame: From Baseline up to approximately 5 years ]

    Percentage change from baseline in the sum of target lesion volume, MRI-measurable non-target lesion volume and all MRI measurable (target an non-target) lesion volume as assessed by BIRC.

    Target lesions are defined as anatomically reproducibly defined tissue(s) masses, which may be composed of one or several tissue types, and can be accurately measured by imaging technique MRI. Target lesion(s) (up to 3) should be identified at screening, be at least 2 cm in the longest diameter at baseline (for each selected lesion) and may be further reproducibly assessed by MRI.

    MRI-measurable non-target lesions are defined as all anatomic lesions other than selected as target and may be measured at radiologic assessment (at least 2 cm in the longest diameter at baseline, the volume may be further reproducibly assessed by MRI).


  11. Proportion of participants with changes from baseline in other non-target lesions in Group 1 and Group 2 [ Time Frame: From Baseline up to approximately 5 years ]

    Percentage change from baseline in other non-target lesions (by BIRC). Non Target lesions are defined as:

    • Anatomic lesions, limb/trunkal areas affected by PROS, organomegaly when they may be measured only by caliper/ruler (e.g., circumference of changed limb or body part)
    • Truly non-measurable lesions (e.g., small lesions less than 2 cm on MRI, superficial visual lesions, masses, organomegaly, PROS-related enlargement of anatomic area identified by physical exam that is not measurable by reproducible imaging technique)

  12. Proportion of participants with new lesions in Group 1 and Group 2 [ Time Frame: From Baseline up to approximately 5 years ]
    The proportion of patients with new lesions (as assessed by BIRC) will be assessed throughout the study.

  13. Pharmacokinetics (PK) of alpelisib in Group 1 and Group 2: Maximum Concentration (Cmax) [ Time Frame: Week 17 Day 1 (Pre-dose, 1h post dose, 3h post dose, 5h post dose, 8h post dose , 24h post dose/ Pre-dose of Day 2), Week 20 Day 1 (Pre-dose, 3h post dose) and after Week 28, on Day 1 (Pre-dose and 3h post dose) 4 weeks after the first dose escalation ]
    Maximum concentration of alpelisib following drug administration will be assessed for Group 1 and Group 2. After Week 28, blood samples will be collected only for participants who had dose escalation at next scheduled visit 4 weeks after the first dose escalation.

  14. Pharmacokinetics (PK) of alpelisib in Group 1 and Group 2: Trough concentration (Ctrough) [ Time Frame: Week 17 Day 1 (Pre-dose and 24 h post dose/ Pre-dose of Day 2), Week 20 Day 1 (Pre-dose) and after Week 28, on Day 1 (Pre-dose) 4 weeks after the first dose escalation ]
    The trough observed concentration of alpelisib will be assessed for Group 1 and Group 2. After Week 28, blood samples will be collected only for participants who had dose escalation at next scheduled visit 4 weeks after the first dose escalation.

  15. Proportion of participants with healthcare visit/hospitalized due to PROS in Group 1 and Group 2 [ Time Frame: From Baseline up to approximately 5 years ]
    Proportion of participants with healthcare visit/hospitalized due to PROS will be assessed for Group 1 and Group 2.

  16. Proportion of participants requiring rescue surgery due to PROS in Group 1 and Group 2 [ Time Frame: From Baseline up to approximately 5 years ]
    Proportion of participants requiring rescue surgery due to PROS will be assessed for Group 1 and Group 2.

  17. Change from Baseline until End of Treatment in patient-reported pain assessed by Brief Pain Inventory (BPI) Worst Pain intensity item or Wong-Baker Faces Scale (age appropriate) in Group 1 and Group 2 [ Time Frame: From Baseline up to approximately 5 years ]
    Change in scores from Brief Pain Inventory (BPI) items, or Wong-Baker Faces Scale (age appropriate). The BPI item that assesses worst pain intensity in the past 24 hours will be used to assess pain intensity for adult participants (≥18 years old) and pediatric participants (≥12 years old). Participants respond to the item on an 11-point numerical rating scale ranging from 0 (no pain) to 10 (pain as bad as you can imagine). For children under 12, the Wong-Baker Faces Scale will be used in place of the BPI worst pain intensity item. This scale is a single-item that includes drawings of 6 faces that are associated with both a numeric rating and a descriptor (ranging from 0/no hurt - 10/hurts worst)

  18. Changes from Baseline until End of Treatment in patient-reported health-related quality of life assessed by PROMIS-profile (Patient Reported Outcome Measurement Information System) for Group 1 and Group 2 [ Time Frame: From Baseline up to approximately 5 years ]
    Change in scores from the PROMIS-profile (Patient Reported Outcome Measurement Information System). The PROMIS Profiles are a group of PROMIS short forms measuring different domains of health-related quality of life (physical function, fatigue, ability to participate in social/peer relationships, pain interference, pain severity, anxiety, depression and sleep disturbance). All items include 5 response options, except for the pain intensity item, which has 11 response options.

  19. Changes from Baseline until End of Treatment in patient-reported overall impression of symptoms assessed by Patient Global Impression of Symptom Severity (PGIS) for Group 1 and Group 2 [ Time Frame: From Baseline up to approximately 5 years ]
    Change in PGIS item. The PGIS is a single item to assess the participant's perception in the severity of their symptoms using a 5-point verbal rating scale, from "No symptoms" to "Very Severe".



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   2 Years and older   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Signed informed consent and assent (when applicable) from the patient, parent, or guardian prior to any study related screening procedures are performed
  2. Patients with diagnosis of PROS with symptomatic and /or progressive overgrowth and at least one measurable PROS-related lesion confirmed by blinded independent review committee (BIRC) assessment
  3. Documented evidence of a somatic mutation(s) in the PIK3CA gene performed in local laboratories
  4. A tissue sample must be available to be sent to a Novartis-designated central laboratory
  5. Karnofsky (in patients > 16 years old at study entry)/Lansky (≤16 yrs of age at study entry) performance status index ≥50 within 7 days before study treatment start
  6. Adequate bone marrow and organ function including Fasting plasma glucose (FPG) ≤ 140 mg/dL (7.7 mmol/L)* and Glycosylated hemoglobin (HbA1c) ≤ 6.5% (both criteria have to be met) (as assessed by central laboratory for eligibility within 7 days before study treatment start)
  7. Presence of at least one PROS-related measurable lesion defined as a lesion with longest diameter ≥2 cm, when the volume can be accurately and reproducibly measured by MRI, and associated with complaints, clinical symptoms or functional limitations affecting the patient's everyday life. Measurability must be confirmed by BIRC before randomization.

Exclusion Criteria:

  1. Participant with only isolated macrodactyly, skin nevus/nevi and macroencephaly (the only clinical feature or a combination of any of three of them), in absence of other PROS-related lesions at the time of informed consent
  2. Previous treatment with alpelisib and/or any other PI3K inhibitor(s) (except treatment attempt, defined as the attempt to treat PROS with any of PI3K inhibitors, with treatment duration less than 2 weeks and stopped at least 4 weeks prior to the first dose of study medication with alpelisib)
  3. Radiation exposure for PROS treatment purpose within the previous 12 months on those PROS areas which are expected to qualify for target lesions (except lesion(s) progressing after completion of radiotherapy) at time of informed consent.
  4. Debulking or other major surgery performed within 3 months at time of informed consent
  5. Clinically meaningful PROS-related thrombotic event (Grade 2 and more as per CTCAE v.4.03) within 30 days before informed consent, and/or sclerotherapy/embolization for vascular complications performed within 6 weeks before informed consent. Participants (receiving anticoagulants for PROS-related coagulopathy, primary or secondary prophylaxis of thrombosis may be included in the study)
  6. Participants with documented pneumonitis or interstitial lung disease at time of informed consent
  7. History of acute pancreatitis within 1 year before informed consent or past medical history of chronic pancreatitis at time of informed consent
  8. Participants with an established diagnosis of type I diabetes mellitus or uncontrolled type II diabetes mellitus at time of informed consent
  9. Known history of seizure, or epilepsy, regardless of relatedness to PROS sprectrum at time of informed consent, when epilepsy is not controlled and/or the patient may not be switched to non-enzyme inducing antiepilectic drug(s) at time of informed consent.

Other inclusion/exclusion criteria may apply


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04589650


Contacts
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Contact: Novartis Pharmaceuticals 1-888-669-6682 novartis.email@novartis.com
Contact: Novartis Pharmaceuticals +41613241111

Sponsors and Collaborators
Novartis Pharmaceuticals
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Responsible Party: Novartis Pharmaceuticals
ClinicalTrials.gov Identifier: NCT04589650    
Other Study ID Numbers: CBYL719F12201
First Posted: October 19, 2020    Key Record Dates
Last Update Posted: October 19, 2020
Last Verified: October 2020

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Novartis ( Novartis Pharmaceuticals ):
PIK3CA-related overgrowth spectrum (PROS)
Alpelisib
BYL719
Adult
Pediatric
Phase II