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Study details
Enrolling now

First in Human Study of TORL-1-23

TORL Biotherapeutics, LLC
NCT IDNCT05103683ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

90

Study length

about 5 years

Ages

18+

Locations

9 sites in CA, KY, MN +4

What this study is about

Researchers are testing a new medication called TORL-1-23 to see if it's safe and effective for people with advanced cancer. The trial will last about 18 months and involve approximately 90 participants.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take TORL-1-23

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Incidence and severity of adverse events and serious adverse events, Maximum Tolerated Dose (MTD), Recommended Phase 2 Dose (RP2D)

Secondary: 1 Year Overall Survival (1YOS), 2 Year Overall Survival (2YOS), Clearance (CL) of TORL-1-23, Duration of Response (DOR), Maximum Serum Concentration of TORL-1-23 (Cmax), Maximum Serum Concentration of TORL-1-23 at Steady State (Cmax,ss), Objective Response Rate (ORR), Progression Free Survival (PFS)

Body systems

Oncology