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Study details
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A Study of PHN-012 in Patients With Advanced Solid Tumors

Pheon Therapeutics
NCT IDNCT07127874ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

165

Study length

about 2.7 years

Ages

18+

Locations

11 sites in CA, DC, MA +6

What this study is about

This trial is testing a new treatment called PHN-012 for people with advanced solid tumors. The goal is to see if the treatment is safe and effective, as well as how it affects the body's immune system and how it moves through the body.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take PHN-012

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
Standard assignment

Assignment is predetermined by the study protocol.

Extracted study details

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

Endpoints

Primary: Overall response rate (ORR) (Phase 1b), Type, incidence and severity of adverse events (AEs) and serious adverse events (SAEs) (Phase 1a)

Secondary: Best overall response (BOR) (Phase 1a and 1b), Disease control rate (DCR) (Phase 1a and 1b), Overall survival (OS) (Phase 1a and 1b), Pharmacokinetics, AUC of total antibody (Phase 1a and 1b), Pharmacokinetics, AUC of total free payload (Phase 1a and 1b), Pharmacokinetics, Cmax of free payload (Phase 1a and 1b), Pharmacokinetics, Cmax of total antibody (Phase 1a and 1b), Pharmacokinetics, Tmax of free payload (Phase 1a and 1b)

Body systems

Oncology