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Not Yet RecruitingNCT06926998

9MW2821 Combined With Other Antitumor Drugs in Patients With Advanced Gynecological Tumors

An Open-Label, Multicenter Phase Ib/ll Clinical Study Evaluating the Safety and Efficacy of 9MW2821 Combined With Other Antitumor Drugs in Patients With Advanced Gynecological Tumors

Status
Not Yet Recruiting
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
260 (estimated)
Sponsor
Mabwell (Shanghai) Bioscience Co., Ltd. · Industry
Sex
Female
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

To evaluate the safety, tolerability, and preliminary efficacy of 9MW2821 in combination with other anti-tumor agents in patients with advanced gynecological malignancies.

Conditions

Interventions

TypeNameDescription
DRUG9MW2821+other anticancer therapySubjects will receive intravenous (IV) infusion of 9MW2821 +other anticancer therapy as per protocol

Timeline

Start date
2025-04-15
Primary completion
2027-05-01
Completion
2027-05-01
First posted
2025-04-15
Last updated
2025-04-15

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06926998. Inclusion in this directory is not an endorsement.

9MW2821 Combined With Other Antitumor Drugs in Patients With Advanced Gynecological Tumors (NCT06926998) · Clinical Trials Directory