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A Study of HC006 in Subjects With Advanced Solid Tumors - Trial NCT06304571

Access comprehensive clinical trial information for NCT06304571 through Pure Global AI's free database. This Phase 1 trial is sponsored by HC Biopharma Inc. and is currently Recruiting. The study focuses on Advanced Solid Tumor. Target enrollment is 76 participants.

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NCT06304571
Phase 1
Recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06304571
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A Study of HC006 in Subjects With Advanced Solid Tumors
A Phase I, Open-label, Dose-Escalation and Dose-expansion Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, Immunogenicity and Efficacy of HC006 in Advanced Solid Tumor Subjects

Study Focus

Advanced Solid Tumor

HC006

Interventional

drug

Sponsor & Location

HC Biopharma Inc.

Shanghai, China

Timeline & Enrollment

Phase 1

Feb 27, 2024

Jul 16, 2026

76 participants

Primary Outcome

Incidence of Dose Limiting Toxicities(DLTs),Incidence of adverse events(AEs),Incidence of Serious adverse events(SAEs),Clinically Significant changes in safety assessments

Summary

The purpose of this study is to characterize the safety, tolerability, pharmacokinetics (PK),
 Immunogenicity and preliminary antitumor activity of HC006 in subjects with advanced solid
 tumor malignancies. This study is a first-in-human (FIH) study of HC006 in subjects with
 advanced solid tumors.

ICD-10 Classifications

Carcinoma in situ, unspecified
Malignant neoplasm: Prepuce
Malignant neoplasm: Connective and soft tissue, unspecified
Malignant neoplasm: Parametrium
Malignant neoplasm of other connective and soft tissue

Data Source

ClinicalTrials.gov

NCT06304571

Non-Device Trial