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Phase 1/2a Study to Assess the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of WEF-001 as Monotherapy in Advanced KRAS-Mutant Solid Tumours.
Sponsor: Auricula Biosciences Inc.
Summary
This is a study designed to assess the safety, tolerability, pharmacokinetics and preliminary efficacy of WEF-001 as monotherapy in patients with Advanced KRAS-mutant solid tumours.
Official title: An Open-label, Multicenter, Phase 1/2a Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Antitumour Activity of WEF-001 in Participants With Advanced KRAS- Mutant Solid Tumours.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
110
Start Date
2025-07-28
Completion Date
2028-01
Last Updated
2026-01-29
Healthy Volunteers
No
Conditions
Interventions
WEF-001
Starting dose of 0.3 mg/m2 q4wks IV, dose escalation
Locations (4)
NEXT Oncology Dallas
Dallas, Texas, United States
Next Oncology, San Antonio
San Antonio, Texas, United States
Princess Margareth Cancer Center
Toronto, Ontario, Canada
Oxford University Hospital
Headington, Oxford, United Kingdom