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NCT05538572CompletedPhase 1

A Study of PRT3645 in Participants With Select Advanced or Metastatic Solid Tumors

A Phase 1 Open-Label, Multi-Center, Safety and Efficacy Study of PRT3645 in Participants With Select Advanced or Metastatic Solid Tumors

Source: ClinicalTrials.gov · Last updated 1 Jul 2024

Brief summary (registry, in English)

This is a Phase 1 dose-escalation study of PRT3645, a Cyclin-dependent Kinase 4/6 (CDK4/6) inhibitor, in patients with advanced or metastatic solid tumors. The purpose of this study is to investigate the safety, tolerability, dose limiting toxicity, and to determine maximally tolerated dose and recommended phase 2 dose to be used in subsequent development of PRT3645.

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
22 (actual)
First submitted
9 Sept 2022
Start date
27 Dec 2022
Primary completion date
26 Jun 2024
Lead sponsor
Prelude Therapeutics Incorporated
NCT number
NCT05538572

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 22
  • From 27 Dec 2022 to the primary completion date, 26 Jun 2024
  • 13 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Treatment with strong inhibitors of CYP3A4.
  • Endometrial cancer patients who had received prior treatment with a CDK 4/6 inhibitor.

Other illness

  • Participants with advanced, symptomatic, extensive visceral disease.
  • Active inflammatory bowel disease or chronic diarrhea, short bowel syndrome, any upper gastrointestinal surgery including gastric resection, known malabsorption syndrome, or other condition that may impair absorption of PRT3645.
  • History of another malignancy within 3 years except for adequately treated basal cell or squamous cell skin cancer, superficial bladder cancer, prostate intraepithelial neoplasm, carcinoma in situ of the cervix, or other noninvasive or indolent malignancies, or malignancies previously treated with curative intent and not on active therapy or expected to require treatment or recurrence during the study.
  • Clinically significant or uncontrolled cardiac disease, uncontrolled electrolyte disorders, uncontrolled or symptomatic CNS metastases or leptomeningeal disease except for GBM.

Who the study is looking for

  • Histologically confirmed advanced, recurrent, or metastatic solid tumor malignancy that have either progress or ineligible for standard of care therapy:
    • HR+ and HER2- or HR+ and HER2+ breast cancer
    • Recurrent GBM (IDH wild type) or CDKN2A/B homozygous deleted IDH-mutant astrocytoma
    • KRAS-mutant or SMARCA4 loss NSCLC
    • CDK pathway alternation in any of the following tumor types: malignant mesothelioma, HPV-negative HNSCC (including oral cavity, oropharynx, hypopharynx, and larynx), sarcoma, or NSCLC
    • Estrogen receptor positive with TP53 wild type endometrial cancer
  • Willing and able to comply with all scheduled visits, treatment plan, laboratory tests, lifestyle considerations, and other study procedures
  • Must have measurable or non-measureable (but evaluable) disease
  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1 or Karnofsky Performance Status (KPS) ≥80% (KPS is for GBM only)
  • Adequate organ function.
  • Able to swallow and retain oral medication.
  • Must provide either archival or fresh tumor tissue sample during screening.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (13)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
National Cancer Centre Singapore
Coordinator of this site? Confirm its status
SingaporeSingaporeUnknown status
Winship Cancer Institute, Emory University
Coordinator of this site? Confirm its status
AtlantaUnited StatesUnknown status
AdventHealth Medical Group Oncology Research at Celebration
Coordinator of this site? Confirm its status
CelebrationUnited StatesUnknown status
Cleveland Clinic
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ClevelandUnited StatesUnknown status
NEXT Virginia
Coordinator of this site? Confirm its status
FairfaxUnited StatesUnknown status
Miami Cancer Institute
Coordinator of this site? Confirm its status
MiamiUnited StatesUnknown status
Tennessee Oncology, PLLC
Coordinator of this site? Confirm its status
NashvilleUnited StatesUnknown status
Smilow Cancer Hospital Phase 1 Unit
Coordinator of this site? Confirm its status
New HavenUnited StatesUnknown status
Laura and Isaac Perlmutter Cancer Center/ NYU Langone Health
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New YorkUnited StatesUnknown status
Hospital of the University of Pennsylvania
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PhiladelphiaUnited StatesUnknown status
Thomas Jefferson University, Sidney Kimmel Cancer Center
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PhiladelphiaUnited StatesUnknown status
South Texas Accelerated Research Therapeutics, LLC
Coordinator of this site? Confirm its status
San AntonioUnited StatesUnknown status
Florida Cancer Specialists
Coordinator of this site? Confirm its status
SarasotaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.