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Advanced or Metastatic Solid TumorsFirst-in-humanCancerDrugPhase 1

What this study is

This is a Phase 1, first-in-human (FIH), open-label, multicenter study designed to evaluate the safety, tolerability, PK, and preliminary anti-tumor activity of SHY-ONC6 in participants with advanced or metastatic solid tumors who have progressed on or are intolerant to standard therapies. The study will consist of 2 parts: a dose escalation part (Phase 1a) and a dose expansion part (Phase 1b).

What's being tested

  • SHY-ONC6

    Intervention · DRUG

    Participants receive SHY-ONC6 administered orally once daily in 21-day cycles. SHY-ONC6 will be administered until the participant withdraws from study, experiences unacceptable toxicity or other safety event, or their disease progresses.

Study details

Official title
A Phase 1 Multicenter, Open-label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of SHY-ONC6 in Participants With Advanced or Metastatic Solid Tumors
Sponsor
SHY Therapeutics
Conditions
Advanced or Metastatic Solid Tumors · Triple Negative Breast Cancer (TNBC) · HR+ Breast Cancer · Colon Cancer · Gastric Cancer · Hepatecellular Carcinoma · NSCLC (Advanced Non-small Cell Lung Cancer) · Mesothelioma · Pancreatic Carcinoma Metastatic · Hormone Refractory Prostate Cancer · Soft Tissue Sarcomas
Enrolling
30 people
Starts
2026-06-24
Est. completion
2028-05-15
Design
Open-label, single group, Phase 1
Record
View on ClinicalTrials.gov ↗