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Phase I Study of HSK42360-Na in Solid Tumors With BRAF V600 Mutation

NCT07561554 · Status: RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 159

Last updated 2026-05-01

No results posted yet for this study

Summary

This is a phase I, open-label, dose-escalation and expansion study to evaluate the safety, tolerability, PK and PD of HSK42360-Na when given orally in patients with active BRAF V600 mutation locally advanced or metastatic Solid Tumors.

Conditions

  • Solid Tumors (Phase 1)

Interventions

DRUG

HSK42360-Na

Oral administration

Sponsors & Collaborators

  • Haisco Pharmaceutical Group Co., Ltd.

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-03-06
Primary Completion
2028-12-02
Completion
2028-12-02

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07561554 on ClinicalTrials.gov