BG-89894
/ CSPC Pharma, BeOne Medicines
- LARVOL DELTA
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July 03, 2026
An Investigational Study of BG-89894 Tablets in Participants With Advanced Solid Tumors
(clinicaltrials.gov)
- P1 | N=29 | Terminated | Sponsor: BeOne Medicines | Recruiting ➔ Terminated; The study was discontinued following an internal decision by the sponsor
Trial termination • Oncology • Solid Tumor • MTAP
July 03, 2026
An Investigational Study of BGB-58067 As a Single Agent and in Combination With Anticancer Agents in Participants With Advanced Solid Tumors
(clinicaltrials.gov)
- P1 | N=235 | Sponsor: BeOne Medicines | N=97 ➔ 235
Enrollment change • First-in-human • Oncology • Solid Tumor • MTAP
May 07, 2026
BeOne shelves 5 cancer programs…
(FierceBiotech)
- "Four of the five cancer assets have been discontinued entirely, BeOne announced in its May 6 earnings presentation (PDF). These are the EGFR-targeting BG-60366, which was in development for lung cancer; a pan-KRAS inhibitor called BGB-53038 for lung and gastrointestinal tumors; MAT2A inhibitor BG-89894 for lung and solid tumors; and CDK2 inhibitor BG-68501, for breast and solid tumors....A study of the CCR8 antibody BGB-A3055 in solid tumors has also been terminated, but this asset has not been fully discontinued, a BeOne spokesperson confirmed to Fierce Biotech."
Discontinued • Trial termination • Esophageal Adenocarcinoma • Gastric Cancer • Gastroesophageal Junction Adenocarcinoma • Gastrointestinal Cancer • HER2 Negative Breast Cancer • Hormone Receptor Positive Breast Cancer • Lung Non-Squamous Non-Small Cell Cancer • Non Small Cell Lung Cancer • Pancreatic Ductal Adenocarcinoma • Solid Tumor • Triple Negative Breast Cancer
May 13, 2026
An Investigational Study of BGB-58067 As a Single Agent and in Combination With Anticancer Agents in Participants With Advanced Solid Tumors
(clinicaltrials.gov)
- P1 | N=525 | Recruiting | Sponsor: BeOne Medicines | N=244 ➔ 525 | Trial completion date: Jan 2029 ➔ Sep 2027 | Trial primary completion date: Jan 2029 ➔ Sep 2027
Enrollment change • First-in-human • Trial completion date • Trial primary completion date • Oncology • Solid Tumor • MTAP
May 13, 2026
An Investigational Study of BG-89894 Tablets in Participants With Advanced Solid Tumors
(clinicaltrials.gov)
- P1 | N=29 | Terminated | Sponsor: BeOne Medicines | Active, not recruiting ➔ Terminated; The study was discontinued following an internal decision by the sponsor
Trial termination • Oncology • Solid Tumor • MTAP
April 30, 2026
An Investigational Study of BGB-58067 As a Single Agent and in Combination With Anticancer Agents in Participants With Advanced Solid Tumors
(clinicaltrials.gov)
- P1 | N=244 | Recruiting | Sponsor: BeOne Medicines | N=79 ➔ 244
Enrollment change • First-in-human • Oncology • Solid Tumor • MTAP
April 02, 2026
A Phase 1a/b Study Investigating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Antitumor Activity of PRMT5 Inhibitor BGB-58067 Alone and in Combination with Anticancer Agents in Patients With Advanced Solid Tumors
(clinicaltrials.gov)
- P1 | N=63 | Recruiting | Sponsor: BeOne Medicines | N=44 ➔ 63
Enrollment change • First-in-human • Oncology • Solid Tumor • MTAP
March 28, 2026
An Investigational Study of BG-89894 Tablets in Participants With Advanced Solid Tumors
(clinicaltrials.gov)
- P1 | N=29 | Active, not recruiting | Sponsor: BeOne Medicines | Recruiting ➔ Active, not recruiting | N=140 ➔ 29 | Trial completion date: Dec 2028 ➔ Apr 2026
Enrollment change • Enrollment closed • Trial completion date • Oncology • Solid Tumor • MTAP
December 25, 2025
An Investigational Study of BGB-58067 As a Single Agent and in Combination With Anticancer Agents in Participants With Advanced Solid Tumors
(clinicaltrials.gov)
- P1 | N=244 | Recruiting | Sponsor: BeOne Medicines | Trial completion date: Jun 2027 ➔ Jan 2029 | Trial primary completion date: Jun 2027 ➔ Jan 2029
Trial completion date • Trial primary completion date • Oncology • Solid Tumor
September 06, 2025
An Investigational Study of BGB-58067 As a Single Agent and in Combination With Anticancer Agents in Participants With Advanced Solid Tumors
(clinicaltrials.gov)
- P1 | N=237 | Recruiting | Sponsor: BeiGene | N=92 ➔ 237 | Trial completion date: Nov 2026 ➔ Jun 2027 | Trial primary completion date: Nov 2026 ➔ Jun 2027
Enrollment change • Trial completion date • Trial primary completion date • Oncology • Solid Tumor
June 11, 2025
An Investigational Study of BG-89894 Tablets in Participants With Advanced Solid Tumors
(clinicaltrials.gov)
- P1 | N=140 | Recruiting | Sponsor: BeiGene | Trial completion date: Dec 2026 ➔ Dec 2028
Trial completion date • Oncology • Solid Tumor
June 06, 2025
A Phase 1 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Anti-tumor Activity of SYH2039 Tablets in Adults with Advanced Solid Tumors
(ChiCTR)
- P1 | N=186 | Recruiting | Sponsor: Guangdong Provincial People's Hospital(Guangdong Academy of Medical Sciences); Guangdong Provincial People's Hospital(Guangdong Academy of Medical Sci
New P1 trial • Esophageal Cancer • Gastric Cancer • Gastroesophageal Junction Adenocarcinoma • Lung Adenocarcinoma • Lung Cancer • Non Small Cell Lung Cancer • Oncology • Solid Tumor • MTAP
February 18, 2025
Study of SYH2039 in Participants with Advanced Solid Tumors
(clinicaltrials.gov)
- P1 | N=186 | Recruiting | Sponsor: CSPC ZhongQi Pharmaceutical Technology Co., Ltd. | Not yet recruiting ➔ Recruiting
Enrollment open • Oncology • Solid Tumor
December 12, 2024
BeiGene Announces Global Licensing Agreement for MAT2A Inhibitor
(Businesswire)
- "BeiGene...announced it has entered into a global licensing agreement with CSPC Zhongqi Pharmaceutical Technology...for SYH2039, a novel methionine adenosyltransferase 2A (MAT2A)-inhibitor being explored for solid tumors....'This MAT2A inhibitor is a valuable addition to our solid tumor pipeline, and we’re eager to explore its potential, particularly in combination with our internally developed PRMT5 inhibitor, BGB-58067'....BGB-58067, which is on track to enter the clinic before the end of the year, is designed to avoid on-target hematological toxicity seen with first-generation PRMT5 inhibitors....Under the terms of the agreement, BeiGene has an exclusive license to develop, manufacture and commercialize SYH2039 worldwide. CSPC will receive upfront and time-based payments totaling $150 million and will be eligible for payments upon the achievement of certain development and commercial milestones and tiered royalties."
Licensing / partnership • New trial • Solid Tumor
August 23, 2024
Study of SYH2039 in Participants With Advanced Solid Tumors
(clinicaltrials.gov)
- P1 | N=186 | Not yet recruiting | Sponsor: CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
Metastases • New P1 trial • Oncology • Solid Tumor
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