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A Study of AL102 in Patients With Progressing Desmoid Tumors (RINGSIDE)

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ClinicalTrials.gov Identifier: NCT04871282
Recruitment Status : Recruiting
First Posted : May 4, 2021
Last Update Posted : November 5, 2021
Sponsor:
Information provided by (Responsible Party):
Ayala Pharmaceuticals, Inc,

Brief Summary:
The current study is designed to evaluate the efficacy and safety of AL102 in patients with progressive desmoid tumors.

Condition or disease Intervention/treatment Phase
Desmoid Desmoid Tumor Drug: AL102 Other: Placebo Phase 2 Phase 3

Detailed Description:
This is a Phase 2/3, randomized study in subjects with progressive desmoid tumors consisting of 2 parts. Part A is an open-label, dose regimen finding study; Part B is a double blind, placebo-controlled study utilizing the dose regimen selected in Part A.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 192 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Care Provider, Investigator)
Primary Purpose: Treatment
Official Title: RINGSIDE: A Phase 2/3, Randomized, Multicenter Study to Evaluate AL102 in Patients With Progressing Desmoid Tumors
Actual Study Start Date : March 30, 2021
Estimated Primary Completion Date : January 12, 2025
Estimated Study Completion Date : February 21, 2025

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Part A Main Study 1.2 mg daily
AL102 1.2 mg
Drug: AL102
AL102 is an inhibitor of gamma secretase-mediated Notch signaling.

Experimental: Part A Main Study 2 mg Intermittent
AL102 2 mg
Drug: AL102
AL102 is an inhibitor of gamma secretase-mediated Notch signaling.

Experimental: Part A Main Study 4 mg Intermittent
AL102 4 mg
Drug: AL102
AL102 is an inhibitor of gamma secretase-mediated Notch signaling.

Experimental: Part B AL102
AL102, recommended dose regimen from Part A
Drug: AL102
AL102 is an inhibitor of gamma secretase-mediated Notch signaling.

Placebo Comparator: Part B Placebo
Placebo to match recommended dose regimen from Part A
Other: Placebo
Placebo to match AL102




Primary Outcome Measures :
  1. Progression free survival [ Time Frame: Approximately 2 years ]
    Progression free survival (PFS) as defined as the time from randomization until the date of assessment of progression (as assessed by BICR based on RECIST v1.1) or death by any cause


Secondary Outcome Measures :
  1. Overall response rate [ Time Frame: Approximately 2 years ]
    Overall response rate (ORR) defined as the proportion of subjects with ORR (CR and PR) by BICR based on RECIST v1.1.

  2. Duration of response [ Time Frame: Approximately 2 years ]
    Duration of response defined by the time from CR or PR (by BICR based on RECIST v1.1) until the earlier of the first documentation of disease progression or death from any cause.

  3. Patient reported outcome [ Time Frame: Approximately 2 years ]
    Change from baseline in quality of life as measured by GOunder/Desmoid Tumor Research Foundation (DTRF) DEsmoid Symptom Scale and Impact Scale (GODDESS)

  4. Patient reported outcome [ Time Frame: Approximately 2 years ]
    Change from baseline in quality of life as measured by Patient-reported outcomes measurement information system (PROMIS) Physical Function

  5. Patient reported outcome [ Time Frame: Approximately 2 years ]
    Change from baseline in quality of life as measured by EuroQol 5-dimensional questionnaire(EQ-5D)

  6. Patient reported outcome [ Time Frame: Approximately 2 years ]
    Change from baseline in pain assessment using brief pain inventory (BPI) short form



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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria Part A:

  1. At least 18 years of age (inclusive) at the time of signing the ICF.
  2. Histologically confirmed desmoid tumor (aggressive fibromatosis) by local pathologist (prior to informed consent) that has progressed by ≥ 20% as measured by RECIST v1.1 within 12 months of the screening visit scan.
  3. At least 1 measurable lesion amenable to volume measurements by MRI at screening (Part A only)
  4. One of the following:

    • Treatment naïve subjects whose disease is not amenable to surgery without the risk of significant morbidity; OR
    • Recurrent/refractory disease following at least one line of therapy (including surgery, radiation, or systemic therapy).
  5. A desmoid tumor in which continued progressive disease will not result in immediate significant risk to the subject.
  6. Agrees to provide formalin-fixed paraffin embedded archival or fresh tumor tissue for re-confirmation of disease.
  7. Must be able to swallow whole capsules with no GI condition affecting absorption; nasogastric or G-tube administration is not allowed.

Exclusion Criteria Part A:

  1. Diagnosed with a malignancy in the past 2 years.
  2. Current or recent (within 2 months of IP administration) GI disease or disorders that increase the risk of diarrhea, such as inflammatory bowel disease and Crohn's disease.
  3. Evidence of uncontrolled, active infection, requiring systemic anti-bacterial, anti-viral or anti-fungal therapy ≤7 days prior to administration of IP such as known active infection with hepatitis B, hepatitis C, or human immunodeficiency virus (HIV) at Screening.
  4. Myocardial infarction within 6 months prior to enrollment, greater than Class 1 angina pectoris, or has New York Heart Association (NYHA) Class III or IV heart failure, , symptomatic ventricular arrhythmias, sustained ventricular tachycardia, Torsade's de Pointes (TdP), the long QT syndrome, pacemaker dependence, or electrocardiographic evidence of acute ischemia.
  5. Unstable or severe uncontrolled medical condition (e.g., unstable cardiac or pulmonary function or uncontrolled diabetes) or any important medical illness or abnormal laboratory finding that would, in the investigator's judgment, increase the risk to the subject associated with his or her participation in the study.
  6. Pregnant or breastfeeding or expecting to conceive children within the projected duration of the study.
  7. Eastern Cooperative Oncology Group (ECOG) performance status ≥2
  8. Abnormal organ and marrow function at Screening defined as:

    1. Neutrophils <1000/mm3,
    2. Platelet count <100,000/mm3,
    3. Hemoglobin <9 g/dL,
    4. Total bilirubin >1.5x upper limit of normal (ULN) (except known Gilbert's syndrome),
    5. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) >2.5x ULN,
    6. Serum creatinine > ULN and creatinine clearance (CrCl) <60 mL/min (calculation of CrCl will be based on acceptable institution standard)
    7. Uncontrolled triglyceride ≥Grade 2 elevations per common terminology criteria for adverse events (CTCAE) v5.0 (>300 mg/dL or >3.42 mmol/L).
  9. ECG Exclusions (Part A only)

    1. Mean QT interval corrected for heart rate using Fridericia's formula (QTcF) ≥450 msec.
    2. QRS duration > 110 ms
    3. PR interval > 240 ms
    4. Marked ST-T wave abnormalities which would make it difficult to measure the QT interval
  10. Any treatments for desmoid tumors within 4 weeks prior to first dose of investigational therapy; subject must have recovered from therapy related toxicity to < CTCAE Grade 2 or clinical baseline. Therapy includes:

    1. Locoregional tumor directed therapies such as major surgery, radiation, radiofrequency ablation, or cryosurgery
    2. Systemic therapy including chemotherapy, biologic (anti-neoplastic agent, antibodies), TKIs (e.g., sorafenib, pazopanib, imatinib), hormonal therapy, or investigational therapy
  11. Chronic NSAIDs for the treatment of desmoid tumors within 4 weeks of first dose of IP;

Inclusion Criteria Part B

  1. ≥12 years of age (inclusive) and ≥ 40 kg at the time of signing the ICF.
  2. Evidence of measurable disease by CT/MRI scan. Measurable lesions are defined according to RECIST v1.1.
  3. Subject and/or legally authorized representative (i.e. parent/guardian) must be capable of giving signed informed consent, which includes compliance with the requirements and restrictions listed in the ICF.
  4. Minor subjects must be capable of giving written assent as appropriate per the applicable age (per local regulatory requirements).

For all other inclusion criteria refer to Part A inclusion criteria.

Exclusion Criteria Part B The subjects must be excluded from participating in the study if they meet any of the exclusion criteria for Part A, except where otherwise noted.


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): NCT04871282


Contacts
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Contact: Jason Kaplan, MD +1-857-444-0553 clinicaltrials@ayalapharma.com
Contact: Johnathan Yoval, MD clinicaltrials@ayalapharma.com

Locations
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Sponsors and Collaborators
Ayala Pharmaceuticals, Inc,
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Responsible Party: Ayala Pharmaceuticals, Inc,
ClinicalTrials.gov Identifier: NCT04871282    
Other Study ID Numbers: AL-DES-01
First Posted: May 4, 2021    Key Record Dates
Last Update Posted: November 5, 2021
Last Verified: November 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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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 Ayala Pharmaceuticals, Inc,:
RINGSIDE
Additional relevant MeSH terms:
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Fibromatosis, Aggressive
Fibroma
Neoplasms, Fibrous Tissue
Neoplasms, Connective Tissue
Neoplasms, Connective and Soft Tissue
Neoplasms by Histologic Type
Neoplasms