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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 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline through approximately 2 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline through approximately 2 years
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
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Who is running the clinical trial?
Prelude TherapeuticsLead Sponsor
8 Previous Clinical Trials
639 Total Patients Enrolled
Frequently Asked Questions
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