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Not Yet RecruitingNCT06131216

Phase I Study of SHR-2022 Injection in the Treatment of Patients With Advanced Malignant Tumors

Phase I Clinical Study on the Safety, Tolerability, Pharmacokinetics and Efficacy of SHR-2022 Injection Alone or in Combination With Other Anti-tumor Treatments in Patients With Advanced Malignant Tumors

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
116 (estimated)
Sponsor
Suzhou Suncadia Biopharmaceuticals Co., Ltd. · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

To evaluate the safety and tolerability of SHR-2022 in patients with advanced malignancies and to determine MTD or MAD versus RP2D

Conditions

Interventions

TypeNameDescription
DRUGSHR-2022 InjectionSHR-2022 Injection is administered by intravenous (IV) infusion

Timeline

Start date
2023-12-01
Primary completion
2026-12-01
Completion
2026-12-01
First posted
2023-11-14
Last updated
2023-11-14

Source: ClinicalTrials.gov record NCT06131216. Inclusion in this directory is not an endorsement.

Phase I Study of SHR-2022 Injection in the Treatment of Patients With Advanced Malignant Tumors (NCT06131216) · Clinical Trials Directory