MedPath

Betta Pharmaceuticals Co., Ltd.

Betta Pharmaceuticals Co., Ltd. logo
🇨🇳China
Ownership
Joint Venture, Public, Subsidiary
Established
2003-01-07
Employees
1.9K
Market Cap
-
Website
https://www.bettapharma.com

Clinical Trials

73

Active:4
Completed:17

Trial Phases

5 Phases

Phase 1:31
Phase 2:24
Phase 3:9
+2 more phases

Drug Approvals

0

Drug Approvals

No drug approvals found

This company may not have drug approvals in our database

Clinical Trials

Distribution across different clinical trial phases (73 trials with phase data)• Click on a phase to view related trials

Phase 1
31 (42.5%)
Phase 2
24 (32.9%)
Phase 3
9 (12.3%)
Phase 4
8 (11.0%)
Not Applicable
1 (1.4%)

Sequential Chemotherapy With Befotertinib in Non-Small Cell Lung Cancer (NSCLC) Patients With Resistance to Third-Generation EGFR-TKI

Not Applicable
Recruiting
Conditions
NSCLC
Adjuvant Drug Therapy
EGFR
Interventions
First Posted Date
2025-09-18
Last Posted Date
2025-09-30
Lead Sponsor
Betta Pharmaceuticals Co., Ltd.
Target Recruit Count
28
Registration Number
NCT07181499
Locations
🇨🇳

The Cancer Center of The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, Guangdong, China

🇨🇳

Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China

Study of MCLA-129 in the Treatment of Advanced Non-small Cell Lung Cancer with AGA and MET Amplification.

Phase 2
Not yet recruiting
Conditions
Non-Small Cell Lung Cancer
Interventions
First Posted Date
2025-03-20
Last Posted Date
2025-03-20
Lead Sponsor
Betta Pharmaceuticals Co., Ltd.
Target Recruit Count
100
Registration Number
NCT06885840
Locations
🇨🇳

The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China

🇨🇳

The First Hospital of Lanzhou University, Lanzhou, Gansu, China

🇨🇳

Dongguan People's Hospital, Dongguan, Guangdong, China

and more 1 locations

A Phase I Study of CFT8919 in Patients With Advanced NSCLC

Phase 1
Not yet recruiting
Conditions
Non-Small Cell Lung Cancer With EGFR Mutation
Interventions
Drug: Dose-Escalation (Phase Ia) CFT8919 capsule
Drug: Dose-Expansion (Phase Ib) CFT8919 capsule
Drug: Cohort-Expansion (Phase Ic) CFT8919 capsule
First Posted Date
2024-10-15
Last Posted Date
2024-10-15
Lead Sponsor
Betta Pharmaceuticals Co., Ltd.
Target Recruit Count
166
Registration Number
NCT06641609
Locations
🇨🇳

浙江省杭州市拱墅区半山东路1号的英文翻译为: No. 1 Banshan East Road, Gongshu District, Hangzhou, Zhejiang Province, China, Hangzhou, Zhejiang, China

A Study To Evaluate The Effect Of Rifampicin Or Ltraconazole On Pharmacokinetics Of Ensartinib In Healthy Volunteers

Phase 1
Not yet recruiting
Conditions
Healthy
Interventions
First Posted Date
2024-07-09
Last Posted Date
2024-07-09
Lead Sponsor
Betta Pharmaceuticals Co., Ltd.
Target Recruit Count
36
Registration Number
NCT06492525
Locations
🇨🇳

The Second Affiliated hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, China

Adjuvant Befotertinib in Stage IB-IIIB Non-small Cell Lung Cancer With Positive EGFR Sensitive Mutations

Phase 3
Recruiting
Conditions
Non-Small Cell Lung Cancer
EGFR Sensitive Mutation
Adjuvant Therapy
Interventions
First Posted Date
2023-09-18
Last Posted Date
2023-09-22
Lead Sponsor
Betta Pharmaceuticals Co., Ltd.
Target Recruit Count
570
Registration Number
NCT06041776
Locations
🇨🇳

Peking University International Hospital, Beijing, China

🇨🇳

Jiangsu Cancer Hospital, Nanjing, China

🇨🇳

Shanghai chest hospital, Shanghai, China

  • Prev
  • 1
  • 2
  • 3
  • 4
  • 5
  • 15
  • Next

News

EyePoint Pharmaceuticals Raises $150 Million to Advance DURAVYU Phase 3 Trials for Retinal Diseases

EyePoint Pharmaceuticals announced a $150 million public offering to fund clinical development of DURAVYU for wet age-related macular degeneration and diabetic macular edema.

Angel Pharmaceuticals Receives China IND Approval for Soquelitinib Atopic Dermatitis Trial

Angel Pharmaceuticals received IND approval from China's NMPA to initiate a Phase 1b/2 clinical trial of soquelitinib for moderate-to-severe atopic dermatitis treatment.

C4 Therapeutics Announces 2025 Milestones for Oncology-Focused Degrader Medicines

C4 Therapeutics is set to advance clinical development of cemsidomide, with Phase 1 data expected in late 2025 for multiple myeloma and non-Hodgkin’s lymphoma.

EyePoint's DURAVYU Shows Promise in Phase 2 DME Trial

EyePoint Pharmaceuticals reported positive interim results from its Phase 2 VERONA trial of DURAVYU for diabetic macular edema (DME).

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.