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RECRUITING
NCT07148128
PHASE1/PHASE2

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.

View on ClinicalTrials.gov

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

Interventions

DRUG

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