Phase I/IIa Study of BR1733 in Subjects With Advanced Cancers

NCT ID: NCT05749549

Last Updated: 2024-08-07

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 191 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-04-19
• Study Completion Date: 2026-05-31

Brief Summary

This study is a Phase I/IIa, multi-center, open-label study of BR1733 with a dose escalation part followed by a dose expansion part in adult subjects with advanced cancers.

This treatment to characterize the safety, tolerability, PK, PD and preliminary antitumor activity.

The study treatment will be administered until the subject experiences unacceptable toxicity, progressive disease, and/or has treatment discontinued at the discretion of the Investigator or the subject, or due to withdrawal of consent.

Detailed Description

This is a multi-center, nonrandomized, open-label study to evaluate the safety, tolerability, pharmacokinetics/ pharmacodynamics, and efficacy of BR1733 in patients with advance cancer, such as recurrent/refractory follicular lymphoma, peripheral T cell lymphoma(PTCL), diffuse large B cell lymphoma(DLBCL) and advance solid tumors.

Phase Ⅰ (Dose Escalation Phase): According to the incidence of DLT in BR1733 tablets in the treatment of advanced cancers, MTD and the Phase 2 clinical trial dose (RP2D) combining PK, PD, efficacy and safety data were determined.

Phase IIa (Dose expansion stage): Evaluate the efficacy and safety of BR1733 monotherapy (Cohorts 1-5) in five separate cohorts.

Conditions

Advanced Cancer; Follicular Lymphoma; Peripheral T Cell Lymphoma; Diffuse Large B Cell Lymphoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

BR1733

25-1200 mg QD or BID

Group Type: EXPERIMENTAL

BR1733

Intervention Type: DRUG

Subjects will receive oral administration of BR1733.

Interventions

BR1733

Subjects will receive oral administration of BR1733.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Sign informed consent voluntarily.

2. Subjects with PTCL, DLBCL or advance solid tumors diagnosed by histology or cytology，whose disease progressed after standard treatment or have no standard treatment.

3. ECOG≤2.

4. Expected survival period ≥ 3 months.

5. Adequate organ function reserve at baseline.

Exclusion Criteria

1. Subjects with symptomatic central nervous system (CNS) metastases or carcinomatous meningitis;

2. Subjects with a history of other primary malignancies within 5 years (except for cured cervical carcinoma in situ, non-melanoma skin cancer, and superficial bladder tumor), subjects with other primary tumors who had no evidence of disease for 5 years or more and did not require treatment could participate in the study;

3. Subjects with any severe uncontrolled disease such as liver disease such as cirrhosis, decompensated liver disease, kidney failure needs for hemodialysis or peritoneal dialysis, etc.

4. Subjects with HIV disease or a positive HIV test; or active hepatitis.

5. Subjects with organ transplantation (apart from keratoplasty) or allogeneic hematopoietic stem cell transplantation.

6. Subjects with impaired or clinically significant cardiac cerebrovascular disease.

7. Subjects known to be allergic to experimental drugs or similar compounds.

8. Subjects known with psychotropic substance abuse, alcohol or drug abuse, or mental disorders.

9. Any previous treatment with other EED inhibitors (e.g., MAK683, FTX-6058, etc.).

10. Females who are pregnant or breastfeeding.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Shanghai Blueray Biopharma Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College

Tianjin, , China

Countries

China

Other Identifiers

BR1733-101

Identifier Type: -

Identifier Source: org_study_id