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MCL1 Inhibitor

PRT1419 for Non-Hodgkin's Lymphoma

Phase 1
Waitlist Available
Research Sponsored by Prelude Therapeutics
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline through approximately 2 years
Awards & highlights

Study Summary

This trial is testing a new cancer drug to see what the best dose is and if it has any side effects.

Eligible Conditions
  • Non-Hodgkin's Lymphoma
  • Myelodysplastic Syndrome
  • Multiple Myeloma
  • Acute Myeloid Leukemia

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline through approximately 2 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline through approximately 2 years for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
To describe dose limiting toxicities (DLT) of PRT1419
To determine the maximally tolerated dose (MTD) and/or optimal biological dose (OBD)
To determine the recommended phase 2 dose (RP2D) and schedule of PRT1419
Secondary outcome measures
To describe any anti-tumor activity of PRT1419
To describe the adverse event profile and tolerability of PRT1419
To describe the pharmacokinetic profile of PRT1419

Trial Design

1Treatment groups
Experimental Treatment
Group I: PRT1419Experimental Treatment1 Intervention
PRT1419 will be administered orally
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
PRT1419
2020
Completed Phase 1
~50

Find a Location

Who is running the clinical trial?

Prelude TherapeuticsLead Sponsor
8 Previous Clinical Trials
639 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~4 spots leftby Apr 2025