Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT07469891 · ClinicalTrials.gov registry record · Phase 1

A Phase 1 Study of PRT12396 in Participants With Select Myeloproliferative Neoplasms

A Phase 1 study, sponsored by Prelude Therapeutics.

Recruiting
Registry status
Phase 1
Development phase
100
Enrollment target

NCT07469891: Recruiting Phase 1 study, sponsored by Prelude Therapeutics.

NCT07469891 is a Phase 1 study that is actively recruiting participants, run by Prelude Therapeutics. The registered enrollment target is 100 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07469891, a Phase 1 study, is actively recruiting participants, sponsored by Prelude Therapeutics.

RECRUITING
Registry status
Phase 1
Development phase
100 participants
Enrollment target

Study Summary

This is a first-in-human, open-label, multi-center Phase 1 study designed to evaluate the safety, tolerability, pharmacokinetics, and preliminary efficacy of PRT12396 in participants with high-risk polycythemia vera (PV) and myelofibrosis (MF), and to determine the maximum tolerated dose (MTD) and recommended dose(s) for expansion (RDE\[s\]). The study consists of a dose-escalation phase followed by a dose-expansion phase to further evaluate selected dose level(s).

Primary Outcome

Incidence of dose limiting toxicities, defined according to protocol-specified criteria

Interventions

  • DRUG PRT12396

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2026-04-29
Est. Completion 2028-04
Phase Phase 1
Prelude Therapeutics

12 total trials

What NCT07469891 shows while recruiting

NCT07469891 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% higher).

The record links to 0 conditions, and to 1 intervention - of which PRT12396 is the first listed.

NCT07469891 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07469891 about?

NCT07469891 is a clinical study titled "A Phase 1 Study of PRT12396 in Participants With Select Myeloproliferative Neoplasms". This is a first-in-human, open-label, multi-center Phase 1 study designed to evaluate the safety, tolerability, pharmacokinetics, and preliminary efficacy of PRT12396 in participants with high-risk polycythemia vera (PV) and myelofibrosis (MF), and to determine the maximum tolerated dose (MTD) and r...

What is the current status of trial NCT07469891?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 100 participants. The study started on 2026-04-29. Estimated completion is 2028-04.

What interventions are being tested in trial NCT07469891?

The interventions under investigation include: PRT12396 (DRUG).

Who is sponsoring clinical trial NCT07469891?

This trial is sponsored by Prelude Therapeutics, which has 12 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07469891's enrollment target sits among peer trials

100 546th of 2000 higher than 1,411 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01048281 · 100 participants

    Clinical & Pathological Studies of Upper Gastrointestinal Carcinoma

  • NCT01161199 · 100 participants

    The Use of Leukapheresis to Support HIV Pathogenesis Studies

  • NCT01327690 · 100 participants · Early Phase 1

    Mental Health in Veterans and Families After Group Therapies

  • NCT01730781 · 100 participants

    Imaging Cannabinoid Receptors Using Positron Emission Tomography (PET) Scanning

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT07469891, the US trial registry maintained by the National Library of Medicine. NCT07469891 (mid enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.