Open-Label, Dose-Escalation With Expansion to Assess the Safety, Tolerability, and PK of TRE-515 in Subjects With Solid Tumors

PHASE1RecruitingINTERVENTIONAL
Enrollment

94

Participants

Timeline

Start Date

September 23, 2021

Primary Completion Date

December 31, 2026

Study Completion Date

June 1, 2027

Conditions
Solid Tumor, AdultOncology
Interventions
DRUG

TRE-515

TRE-515 will be administered orally once daily at least 1 hour prior or 2 hours after eating at approximately the same time each day. Dosing will be continuous with no breaks between cycles. Subjects will continue to receive successive cycles of TRE-515 treatment as long as they do not demonstrate progressive disease, experience an unacceptable toxicity, and both the Sponsor and PI consider additional treatment with TRE-515 to be within the best interest of the subject.

Trial Locations (2)

28078

RECRUITING

Carolina BioOncology Institute, Huntersville

90404

RECRUITING

UCLA, Santa Monica

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Trethera

INDUSTRY

NCT05055609 - Open-Label, Dose-Escalation With Expansion to Assess the Safety, Tolerability, and PK of TRE-515 in Subjects With Solid Tumors | Biotech Hunter | Biotech Hunter