DFP-14927 for Advanced Solid Tumors

This study is testing a new drug called DFP-14927 for people with advanced solid tumors (cancers that form in solid organs like the breast or lung) that have not responded to standard treatments or for which no effective treatment is available. DFP-14927 works by targeting the immune system. The main goals are to find the highest safe dose of DFP-14927, understand its side effects, and determine the recommended dose for future studies. You can join if you are 18 or older and have a confirmed solid tumor diagnosis. This study is currently recruiting about 30 participants.

Study design
This is a Phase I, open-label (meaning you and your doctors will know what treatment you are receiving), single-arm study, meaning all participants receive the same treatment. It aims to enroll about 30 participants.
What's involved
You would receive DFP-14927 as an intravenous (IV) infusion weekly for each 28-day cycle. The study will observe drug-related toxicities and dose-limiting toxicities.
Compensation
Not stated in the trial record.
Follow-up
You will be followed from your first dose up to 30 days after your last dose to assess safety and side effects.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT03943004

Trial of DFP-14927 in Advanced Solid Tumors

Recruiting
PHASE1Ages 18+InterventionalTreatment
Delta-Fly Pharma, Inc.
~30 participants
Updated 2025-03-03 on ClinicalTrials.gov
What's tested:DFP-14927

At a glance

Recruiting sites
2 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Determine the maximum tolerated dose (MTD)
Measured over From first dose (Day 1) up to 30 days after last dose
+2 more outcomes measured
Solid Tumor
Cancer
2 sites across 2 states
California1
Texas1
  • Jaffer Ajani, MD · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center

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  • Determine the maximum tolerated dose (MTD)From first dose (Day 1) up to 30 days after last dose

    The highest dose level at which less than one-third of at least 6 patients (i.e., 0 or 1 out of 6) experience a DLT

  • Recommended Phase II Dose (RP2D)From first dose (Day 1) up to 30 days after last dose

    The maximum tolerated dose (MTD) of DFP-14927 at which the Phase II study will explore

  • Dose-Limiting Toxicity (DLT)From first dose (Day 1) up to 30 days after last dose

    Determined through the frequency/severity of adverse events per CTCAE V5.0