Study of BGB-11417 Monotherapy in Participants With Relapsed or Refractory Mantle Cell Lymphoma

Sponsor
BeiGene (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT05471843
Collaborator
(none)
98
1
60

Study Details

Study Description

Brief Summary

The study consists of two parts. Part 1 determines the safety and tolerability of BGB-11417 monotherapy, the maximum tolerated dose, and the recommended Phase 2 dose of BGB-11417 monotherapy for relapsed or refractory mantle cell lymphoma. Part 2 evaluates efficacy of BGB-11417 monotherapy at the recommended Phase 2 dose with recommended ramp-up schedule from Part 1.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
98 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Single-Arm, Open-Label, Multicenter Phase 2 Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Bcl-2 Inhibitor BGB-11417 in Patients With Relapsed or Refractory Mantle Cell Lymphoma
Anticipated Study Start Date :
Aug 1, 2022
Anticipated Primary Completion Date :
Mar 1, 2024
Anticipated Study Completion Date :
Aug 1, 2027

Arms and Interventions

Arm Intervention/Treatment
Experimental: Single Arm

Participants will receive BGB-11417

Drug: BGB-11417
Administered orally

Outcome Measures

Primary Outcome Measures

  1. Part 1: Number Of Participants Experiencing Dose-limiting Toxicities (DLTs) [Up to 1 Year]

  2. Part 1: Number of Participants Reporting One or More Treatment-emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs) [Up to 5 Years]

    with adverse events leading to discontinuation, and AEs graded according NCI-CTCAE Version 5

  3. Part 1: Number of participants experiencing tumor lysis syndrome (TLS) relevant events [Up to 5 Years]

  4. Part 2: Overall Response Rate (ORR) as assessed by the Independent Review Committee (IRC) [Up to 4 Years]

    Defined as the proportion of participants who achieved a stringent complete response (sCR), complete response (CR), very good partial response (VGPR), or partial response (PR) per the Lugano Classification

Secondary Outcome Measures

  1. Part 1:Area Under the Plasma Concentration Time Curve (AUC) [Up to 2 Years]

  2. Part 1:Maximum Observed Plasma Concentration (Cmax) [Up to 2 Years]

  3. Part 1: Time to reach Cmax (Tmax) [Up to 2 Years]

  4. Part 1: Steady State Area Under the Plasma Concentration Time Curve (AUC) [Up to 2 Years]

  5. Part 1: Steady State Maximum Observed Plasma Concentration (Cmax) [Up to 2 Years]

  6. Part 1: Steady State Trough Plasma Concentration (CTrough) [Up to 2 Years]

  7. Part 1: Steady State Time to reach Cmax (Tmax) [Up to 2 Years]

  8. Overall Response Rate (ORR) as assessed by investigator [Up to 4 Years]

    Defined as the proportion of participants who achieved a complete response (CR), or partial response (PR) per Lugano classification

  9. Duration of Response (DOR) as assessed by investigator and IRC [Up to 4 Years]

    DOR is defined as the time from the date of the first documented response (PR or better) after treatment initiation until the date of first documented disease progression or death due to any cause; whichever occurs first

  10. Progression Free Survival (PFS) as assessed by investigator and IRC [Up to 4 Years]

    PFS is defined as the time from the date of the first study dose until the date of first documented disease progression or death due to any cause, whichever occurs first.

  11. Time to Response (TTR) as assessed by investigator and IRC [Up to 4 Years]

    TTR is defined as the time from start of treatment to first documentation of response of Partial Response (PR) or better

  12. Overall Survival (OS) [Up to 4 Years]

    defined as time from the start of treatment to the date of death due to any cause

  13. Part 2: Number of Participants Experiencing Adverse Events (AEs) [Up to 4 Years]

  14. Part 2: Number of participants with clinically significant changes from baseline in vital signs [Up to 4 Years]

    Vital signs include blood pressure and pulse rate

  15. Part 2: Number of participants with clinically significant changes from baseline in clinical laboratory values [Up to 4 Years]

    Laboratory values include hematology, clinical chemistry, coagulation, and urinalysis

  16. Number of Participants With Clinically Significant Physical Examination Findings [Up to 4 Years]

    A full physical examination includes head, ears, eyes, nose, mouth, skin, heart and lung examinations, lymph nodes, gastrointestinal and musculoskeletal systems

  17. Participant Reported Outcomes as measured by NFLymSI-18 [Up to 4 Years]

    The National Comprehensive Cancer Network/Functional Assessment of Cancer Therapy Lymphoma Cancer Symptom Index-18 (FLymSI-18) questionnaire contains 18 items, each of which utilizes a Likert scale with 5 possible responses ranging from 0 'Not at all' to 4 'Very much' and is divided into a total score.

  18. Participants Reported Outcome as measured by EQ-5D-5L questionnaires [Up to 4 Years]

    The EQ-5D-5L descriptive system assesses health in five dimensions (MOBILITY, SELF-CARE, USUAL ACTIVITIES, PAIN / DISCOMFORT, ANXIETY / DEPRESSION), each of which has five levels of response (no problems, slight problems, moderate problems, severe problems, extreme problems/unable to). This part of the EQ-5D questionnaire provides a descriptive profile that can be used to generate a health state profile. Health state index scores generally range from less than 0 (where 0 is the value of a health state equivalent to dead; negative values representing values as worse than dead) to 1 (the value of full health), with higher scores indicating higher health utility. The second part of the questionnaire consists of a visual analogue scale (VAS) on which the participant rates his/her perceived health from 0 (the worst imaginable health) to 100 (the best imaginable health).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Key Inclusion Criteria:
  1. Histologically confirmed diagnosis of MCL

  2. Prior systemic treatments for MCL (at least one line of anti-cluster of differentiate 20 (CD20) based immune or chemoimmunotherapy and at least one line of treatment with Bruton Tyrosine Kinase Inhibitor (BTKi) as mono- or combination therapy)

  3. relapsed/refractory disease

  4. Presence of measurable disease

  5. Availability of archival tissue confirming diagnosis of MCL, or willing to undergo fresh tumor biopsy

  6. Eastern Cooperative Oncology Group (ECOG) performance status of 0,1 or 2.

  7. Adequate organ function

Key Exclusion Criteria:
  1. Known central nervous system involvement by lymphoma

  2. Prior malignancy other than MCL within the past 3 years, except for curatively treated basal or squamous cell skin cancer, superficial bladder cancer, carcinoma in situ of the cervix or breast, or localized Gleason score 6 prostate cancer.

  3. Prior exposure to a Bcl-2 inhibitor (eg, venetoclax/ABT-199).

  4. Prior autologous stem cell transplant within the last 3 months; or prior chimeric cell therapy within the last 3 months; or prior allogeneic stem cell transplant within the last 6 months or currently has an active graft-vs-host disease requiring the use of immunosuppressants.

  5. Clinically significant cardiovascular disease.

  6. Major surgery or significant injury ≤ 4 weeks prior to start of study treatment.

  7. Active fungal, bacterial or viral infection requiring systemic treatment.

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • BeiGene

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
BeiGene
ClinicalTrials.gov Identifier:
NCT05471843
Other Study ID Numbers:
  • BGB-11417-201
  • U1111-1279-0851
First Posted:
Jul 25, 2022
Last Update Posted:
Jul 27, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by BeiGene
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 27, 2022