Trials / Recruiting
RecruitingNCT07296341
HRS-4642 Combination With Other Antitumor Therapies in Patients With Solid Tumors
A Phase IB/II Study To Evaluate the Safety, Tolerability, and Preliminary Efficacy of HRS-4642 Combination With Other Antitumor Therapies in Patients With Solid Tumors
- Status
- Recruiting
- Phase
- Phase 1 / Phase 2
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- Sponsor
- Shanghai Hengrui Pharmaceutical Co., Ltd. · Industry
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
This study is a randomized, open-label, multicenter Phase II clinical trial designed to evaluate the Safety, Tolerability and Preliminary Efficacy of HRS-4642 Combination with Other Antitumor Therapies in Patients with Solid Tumors
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | HRS-4642;Adebrelimab Injection; nab-paclitaxel; gemcitabine | HRS-4642 combination with Adebrelimab Injection, nab-paclitaxel in combination with gemcitabine |
| DRUG | HRS-4642;nab-paclitaxel; gemcitabine | nab-paclitaxel in combination with gemcitabine |
Timeline
- Start date
- 2026-01-08
- Primary completion
- 2027-10-01
- Completion
- 2027-12-01
- First posted
- 2025-12-22
- Last updated
- 2026-01-14
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT07296341. Inclusion in this directory is not an endorsement.