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
Sites (13)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| National Cancer Centre Singapore Coordinator of this site? Confirm its status | Singapore | Singapore | Unknown status |
| Winship Cancer Institute, Emory University Coordinator of this site? Confirm its status | Atlanta | United States | Unknown status |
| AdventHealth Medical Group Oncology Research at Celebration Coordinator of this site? Confirm its status | Celebration | United States | Unknown status |
| Cleveland Clinic Coordinator of this site? Confirm its status | Cleveland | United States | Unknown status |
| NEXT Virginia Coordinator of this site? Confirm its status | Fairfax | United States | Unknown status |
| Miami Cancer Institute Coordinator of this site? Confirm its status | Miami | United States | Unknown status |
| Tennessee Oncology, PLLC Coordinator of this site? Confirm its status | Nashville | United States | Unknown status |
| Smilow Cancer Hospital Phase 1 Unit Coordinator of this site? Confirm its status | New Haven | United States | Unknown status |
| Laura and Isaac Perlmutter Cancer Center/ NYU Langone Health Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Hospital of the University of Pennsylvania Coordinator of this site? Confirm its status | Philadelphia | United States | Unknown status |
| Thomas Jefferson University, Sidney Kimmel Cancer Center Coordinator of this site? Confirm its status | Philadelphia | United States | Unknown status |
| South Texas Accelerated Research Therapeutics, LLC Coordinator of this site? Confirm its status | San Antonio | United States | Unknown status |
| Florida Cancer Specialists Coordinator of this site? Confirm its status | Sarasota | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.