Ovarian Cancer Clinical Trials in Philadelphia, Pennsylvania
25 studies are recruiting for ovarian cancer in Philadelphia, Pennsylvania right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies now recruiting
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Polygenic Risk Scores and Multi-cancer Early Detection for Ovarian Cancer
The overall goal of the Polygenic Risk Scores and Multi-cancer Early Detection for Ovarian Cancer (PROMISE) study is to better understand how women may incorporate both polygenic risk score (PRS) and novel early detection strategies in their decisions regarding cancer screening and risk reducing su…
- Stage
- Not phased
- Ages
- 25 and older
- Site
- Abramson Cancer Center, Philadelphia, Pennsylvania
- Run by
- Abramson Cancer Center at Penn Medicine
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A Study With NKT3964 for Adults With Advanced/Metastatic Solid Tumors
The goal of the Monotherapy Dose Escalation phase (Part 1) of the study is to evaluate the safety, tolerability, pharmacokinetics (PK) and preliminary anti-tumor activity to determine the preliminary recommended dose for expansion (RDE) of NKT3964 in adults with advanced or metastatic solid tumors.…
- Stage
- Phase 1
- Ages
- 19 and older
- Site
- Sidney Kimmell Cancer Center - Jefferson Health, Philadelphia, Pennsylvania
- Locations
- 20 in total
- Run by
- NiKang Therapeutics, Inc.
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A Phase 1 Study of LNCB74 in Advanced Solid Tumors
This is an open-label, phase 1, dose escalation and dose expansion study to determine safety and tolerability, and to determine the maximum tolerated dose and / or recommended phase 2 dose of LNCB74 in participants with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sidney Kimmel Comprehensive Center at Jefferson, Philadelphia, Pennsylvania
- Locations
- 17 in total
- Run by
- LigaChem Biosciences, Inc.
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A Study of ART0380 for the Treatment of Advanced or Metastatic Solid Tumors
This clinical trial is evaluating a drug called ART0380 in participants with advanced or metastatic solid tumors. The main goals of this study are to: * Find the recommended dose of ART0380 that can be given safely to participants alone and in combination with gemcitabine or irinotecan * Learn more…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Pennsylvania / Abramson Cancer Center, Philadelphia, Pennsylvania
- Locations
- 88 in total
- Run by
- Artios Pharma Ltd
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A Phase I/II, First-in-Human Study to Evaluate TJ102 in Participants With Advanced or Metastatic Ovarian Cancer and Other Solid Tumors.
The goal of this clinical trial is to evaluate whether TJ102, an investigational antibody-drug conjugate (ADC), can safely and effectively treat patients with advanced ovarian or other solid tumors. The main objectives of this study are : • To Determine the maximum tolerated dose (MTD) and recommen…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sidney Kimmel Cancer Center Jefferson Health, Philadelphia, Pennsylvania
- Locations
- 9 in total
- Run by
- Phrontline Biopharma
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A Trial to Evaluate Safety, Tolerability, and Preliminary Efficacy of Misetionamide (GP-2250) as Monotherapy or in Combination With Gemcitabine
This is a phase 1 dose escalation trial of monotherapy misetionamide (also known as GP-2250) currently enrolling patients with platinum-resistant ovarian cancer (PROC) into Part 2 of the study. Part 1 of the study evaluating misetionamide in combination with gemcitabine in subjects with advanced pa…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Abramson Cancer Center at the University of Pennsylvania, Philadelphia, Pennsylvania
- Locations
- 4 in total
- Run by
- Persevere Therapeutics Inc.
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Risk Reducing Salpingectomy With Delayed Oophorectomy as an Alternative to Risk- Reducing Salpingo-oophorectomy in High Risk-Women to Assess the Safety of Prevention - US Cohort Study
This is a prospective preference study that will evaluate non-inferiority of the innovative treatment (RRS with delayed RRO) as compared to the standard treatment (RRSO) with respect to high grade serous (ovarian) cancer incidence
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Pennsylvania, Philadelphia, Pennsylvania
- Locations
- 11 in total
- Run by
- M.D. Anderson Cancer Center
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A Study to Assess Adverse Events and Change in Disease Activity of Multiple Treatment Combinations With Intravenous Mirvetuximab Soravtansine in Adult Participants With Ovarian Cancer
Ovarian cancer is a lethal disease with an estimated 310,000 new cases and 200,000 deaths experienced worldwide in 2020. The purpose of this study is to assess the adverse events and change in disease activity of mirvetuximab soravtansine with carboplatin, or bevacizumab (Bev), or bev alone in part…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Penn Medicine University of Pennsylvania Health System /ID# 277963, Philadelphia, Pennsylvania
- Locations
- 86 in total
- Run by
- AbbVie
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A Clinical Trial of Sac-TMT in People With Non-HRD Positive Advanced Ovarian Cancer (MK-2870-021)
Researchers are looking for new ways to treat ovarian cancer (OC). Current treatment for OC may start with surgery to remove as much of the cancer as possible. After surgery, people may receive chemotherapy. After chemotherapy, standard care options may include: * Maintenance treatment, which is us…
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Hospital of the University of Pennsylvania ( Site 0071), Philadelphia, Pennsylvania
- Locations
- 167 in total
- Run by
- Merck Sharp & Dohme LLC
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The Evaluation of PC14586 in Patients With Advanced Solid Tumors Harboring a TP53 Y220C Mutation (PYNNACLE)
The Phase 2 monotherapy portion of this study is currently enrolling and will evaluate the efficacy and safety of PC14586 (INN rezatapopt) in participants with locally advanced or metastatic solid tumors harboring a TP53 Y220C mutation. The Phase 1 portion of the study will assess the safety, toler…
- Stage
- Phase 1
- Ages
- 12 and older
- Site
- Abramson Cancer Center of the University of Pennsylvania, Philadelphia, Pennsylvania
- Locations
- 76 in total
- Run by
- PMV Pharmaceuticals, Inc
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DESTINY-PANTUMOUR04
This study will evaluate the effectiveness of T-DXd in patients with HER2-positive (IHC 3+) locally advanced, unresectable, or metastatic solid tumors who have received prior systemic treatment for metastatic or advanced disease and have no satisfactory alternative treatment options in a real-world…
- Stage
- Not phased
- Ages
- 18 to 130
- Site
- Research Site, Philadelphia, Pennsylvania
- Locations
- 18 in total
- Run by
- AstraZeneca
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A Study to Find Out How Safe REGN5668 is and How Well it Works In Adult Women When Given With Either Cemiplimab, or Cemiplimab + Fianlimab, or Ubamatamab
This study is researching an investigational drug called REGN5668 : * alone or, * combined with cemiplimab (also known as REGN2810) or, * combined with both cemiplimab and fianlimab (also known as REGN3767), or * combined with ubamatamab (also known as REGN4018), with or without sarilumab. The main…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania
- Locations
- 28 in total
- Run by
- Regeneron Pharmaceuticals
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Prehabilitation in High-risk Oncologic Surgery
The goal of this clinical study is to learn whether a prehabilitation program can improve recovery after major abdominal surgery in adults with cancer who are receiving treatment before surgery. Prehabilitation is supportive care given before surgery to help patients prepare physically, nutritional…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Fox Chase Cancer Center - Philadelphia, Philadelphia, Pennsylvania
- Run by
- Fox Chase Cancer Center
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BI-1808 as a Single Agent and With Pembrolizumab (KEYTRUDA® ) in Treatment of Advanced Malignancies(Keynote-D20)
The goal of this first in human clinical trial is to test BI-1808 administered as single agent and in combination with pembrolizumab in subjects with advanced malignancies whose disease has progressed after standard therapy. The main questions it aims to answer are: * how safe and tolerable is BI-1…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Pennsylvania, Philadelphia, Pennsylvania
- Locations
- 25 in total
- Run by
- BioInvent International AB
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FT836 With or Without Chemotherapy and/or Monoclonal Antibodies, in Participants With Advanced Solid Tumors
This is a Phase 1 study of FT836 administered in participants with advanced solid tumors. The primary objectives of the study are to evaluate the safety and tolerability of FT836 with or without chemotherapy and/or trastuzumab or cetuximab, and to determine the recommended phase 2 dose (RP2D) of FT…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Thomas Jefferson University, Sidney Kimmel Cancer Center, Philadelphia, Pennsylvania
- Locations
- 5 in total
- Run by
- Fate Therapeutics
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A Phase 1 Study of NRM-823 in Participants With Locally Advanced or Metastatic Refractory Solid Tumors
This study is being done to find out of NRM-823 is safe and can treat participants with locally advanced or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Normunity Investigational Site, Philadelphia, Pennsylvania
- Locations
- 18 in total
- Run by
- Normunity AccelCo, Inc.
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A Study of Azenosertib (ZN-c3) Versus Investigator's Choice Chemotherapy in Subjects With Platinum-Resistant High-Grade Serous Ovarian, Primary Peritoneal, or Fallopian Tube Cancers Positive for Cyclin E1 Protein Expression
This is a randomized, Phase 3 trial designed to evaluate the efficacy and safety of azenosertib compared to Investigator's choice of chemotherapy in subjects with platinum-resistant ovarian cancer whose tumors are positive for cyclin E1 protein expression.
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Site 0109, Philadelphia, Pennsylvania
- Locations
- 59 in total
- Run by
- K-Group, Beta, Inc., a wholly owned subsidiary of Zentalis Pharmaceuticals, Inc
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Study of Orally Administered MOMA-313 in Participants With Advanced or Metastatic Solid Tumors
This Phase 1, multi-center, open-label, dose escalation and dose optimization study is designed to assess the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PDx), and preliminary clinical activity of MOMA-313 administered orally as a single agent or combination therapy in patients w…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Investigative Site #109, Philadelphia, Pennsylvania
- Locations
- 18 in total
- Run by
- MOMA Therapeutics
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SynKIR-110 for Mesothelin Expressing Ovarian Cancer, Cholangiocarcinoma or Mesothelioma
This first-in-human (FIH) trial is designed to assess the safety, feasibility, and potential activity of a single intravenous (IV) dose of SynKIR-110 administered to subjects with mesothelin-expressing advanced ovarian cancer, mesothelioma, and cholangiocarcinoma.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Pennsylvania, Philadelphia, Pennsylvania
- Locations
- 5 in total
- Run by
- Verismo Therapeutics
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Study of NMS-03305293 in Adult Patients With Relapsed Ovarian Cancer
This is a multicenter, open-label Phase Ia/b study on the safety and efficacy of the combination of NMS-03305293 and topotecan in patients with recurrent ovarian cancer, with dose-limiting toxicity (DLT) escalation. The aim of this study is to determine the safety and tolerability, as well as to ev…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Penn Medicine - Perelman Center for Advanced Medicine, Philadelphia, Pennsylvania
- Locations
- 5 in total
- Run by
- Nerviano Medical Sciences
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TUBectomy With Delayed Oophorectomy in High Risk Women to Assess the Safety of Prevention
The aim of the project is to evaluate the risk-reducing salpingectomy with delayed oophorectomy as an alternative for risk-reducing salpingo-oophorectomy in high risk women with respect to ovarian cancer incidence.
- Stage
- Not phased
- Ages
- 25 to 50
- Site
- Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania
- Locations
- 66 in total
- Run by
- University Medical Center Nijmegen
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A Study of PARG Inhibitor ETX-19477 in Patients With Advanced Solid Malignancies
This is a two-part, open-label, multicenter, dose escalation and dose expansion study designed to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PDx), and anti- tumor activity of ETX-19477, a novel reversible small molecule inhibitor of PARG.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Thomas Jefferson University, Sidney Kimmel Comprehensive Cancer Center, Philadelphia, Pennsylvania
- Locations
- 14 in total
- Run by
- 858 Therapeutics, Inc.
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A Study of CLSP-1025 in Adult Patients With Solid Tumors That Harbor the p53 R175H Mutation
Phase 1 dose escalation and expansion study of CLSP-1025, a first-in-class HLA-A*02:01 specific T cell engager (TCE) targeting solid tumors that harbor the p53 R175H mutation.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Thomas Jefferson University, Sidney Kimmel Cancer Center, Philadelphia, Pennsylvania
- Locations
- 21 in total
- Run by
- Clasp Therapeutics, Inc.
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Healthy Volunteers Study
The purpose of this study is to examine the role of the bacterial environments and metabolites in the early detection and prediction of ovarian cancer development. Vaginal swabs and stool samples will be collected from healthy volunteers, or those without a known ovarian cancer diagnosis or genetic…
- Stage
- Not phased
- Ages
- 30 to 50
- Site
- Abramson Cancer Center of the University of Pennsylvania, Philadelphia, Pennsylvania
- Run by
- Abramson Cancer Center at Penn Medicine
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SYNERGY-AI: Artificial Intelligence Based Precision Oncology Clinical Trial Matching and Registry
International registry for cancer patients evaluating the feasibility and clinical utility of an Artificial Intelligence-based precision oncology clinical trial matching tool, powered by a virtual tumor boards (VTB) program, and its clinical impact on pts with advanced cancer to facilitate clinical…
- Stage
- Not phased
- Ages
- Any age
- Site
- Massive Bio SYNERGY-AI site, Philadelphia, Pennsylvania
- Locations
- 68 in total
- Run by
- Massive Bio, Inc.
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.