Ovarian Cancer Clinical Trials in Fairfax, Virginia
31 studies are recruiting for ovarian cancer in Fairfax, Virginia 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.
Search these by distance from you
Studies now recruiting
-
Study of RGT-490 in Patients With PIK3CA-Mutated Advanced Solid Tumors
This is a phase 1/1b, open-label, multicenter study consisting of sequential parts designed to evaluate the safety, tolerability, and effects pharmacokinetic (PK) profile, and antitumor activity of RGT-490, an investigational oral therapy, in adults with locally advanced or metastatic solid tumors …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Virginia, Fairfax, Virginia
- Locations
- 6 in total
- Run by
- Regor Pharmaceuticals Inc.
-
CR-002 in Adult Participants With Locally Advanced or Metastatic Solid Tumors
The purpose of this study is to determine the safety and tolerability of monotherapy CR-002 and to identify the MTD and/or optimal biologic dose and RP2D(s) in participants with locally advanced or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Clinical Study Site, Fairfax, Virginia
- Locations
- 3 in total
- Run by
- Crescent Biopharma, Inc.
-
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
- NEXT Virginia, Fairfax, Virginia
- Locations
- 20 in total
- Run by
- NiKang Therapeutics, Inc.
-
A Phase 1/2 Trial of TER-2013 in Patients With Solid Tumors Harboring AKT/PI3K/PTEN Pathway Alterations
This is a Phase 1/2, open-label, multicenter study evaluating the safety, tolerability, pharmacokinetics, pharmacodynamics and anti-tumor activity of TER-2013 in patients with advanced solid tumors harboring AKT/PI3K/PTEN pathway alterations.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Oncology, Fairfax, Virginia
- Locations
- 25 in total
- Run by
- Terremoto Biosciences Inc.
-
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
- Virginia Cancer Specialists, Fairfax, Virginia
- Locations
- 88 in total
- Run by
- Artios Pharma Ltd
-
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
- NEXT Virginia, Fairfax, Virginia
- Locations
- 9 in total
- Run by
- Phrontline Biopharma
-
Study to Evaluate INCB123667 Versus Investigator's Choice of Chemotherapy in Participants With Platinum-Resistant Ovarian Cancer With Cyclin E1 Overexpression
The purpose of this study is to evaluate INCB123667 versus investigator's choice of chemotherapy in participants with platinum-resistant ovarian cancer with cyclin E1 overexpression.
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Inova Schar Cancer Institute, Fairfax, Virginia
- Locations
- 198 in total
- Run by
- Incyte Corporation
-
Open Label Study to Evaluate BL-M07D1 in HER2 Expressing Malignant Solid Tumors
The objective of this study is to evaluate the safety, tolerability, and efficacy of BL-M07D1 in patients with HER2 expressing advanced tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Virginia Cancer Specialists, Fairfax, Virginia
- Locations
- 26 in total
- Run by
- SystImmune Inc.
-
First-in-Human Study of ATX-295, an Oral Inhibitor of KIF18A, as Monotherapy and in Combination With Anticancer Therapy in Patients With Advanced or Metastatic Solid Tumors, Including Ovarian Cancer
The goal of this study is to identify a safe and tolerated dose of the orally administered KIF18A inhibitor ATX-295. In addition, this study will evaluate the pharmacokinetics, pharmacodynamics and preliminary antitumor activity of ATX-295 as a monotherapy and in combination with bevacizumab (or a …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Virginia, Fairfax, Virginia
- Locations
- 11 in total
- Run by
- Accent Therapeutics
-
A Study to Evaluate the Efficacy and Safety of Sacituzumab Tirumotecan (MK-2870) Maintenance Treatment Versus Standard of Care in Participants With Platinum-sensitive Recurrent Ovarian Cancer (MK-2870-022/TroFuse-022/ENGOT-ov84/GOG-3103)
The main goals of this study are to learn about the safety of sacituzumab tirumotecan with bevacizumab and if people tolerate it; and if people who take sacituzumab tirumotecan with or without bevacizumab live longer without the cancer getting worse than those who receive standard of care treatment.
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Virginia Cancer Specialists (VCS) ( Site 8011), Fairfax, Virginia
- Locations
- 198 in total
- Run by
- Merck Sharp & Dohme LLC
-
A Study to Assess Adverse Events, Change in Disease Activity and How Intravenous (IV) ABBV901 Moves Through the Body Alone or in Combination With Other Anticancer Drugs in Adult Participants With Ovarian Cancer
Ovarian cancer (OC) is a lethal disease. The purpose of this study is to assess the safety, pharmacokinetics and efficacy of ABBV901, alone or in combination with other anticancer drugs, in participants with ovarian cancer. ABBV901 is an investigational drug for the treatment of ovarian cancer. Thi…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Next Virginia /ID# 278607, Fairfax, Virginia
- Locations
- 27 in total
- Run by
- AbbVie
-
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
- Virginia Cancer Specialists (VCS) ( Site 8012), Fairfax, Virginia
- Locations
- 167 in total
- Run by
- Merck Sharp & Dohme LLC
-
Phase I/IIa Study of AZD5335 as Monotherapy and Combination Therapy in Participants With Solid Tumors
This research is designed to determine if experimental treatment with Antibody-drug conjugate, AZD5335, alone, or in combination with anti-cancer agents is safe, tolerable, and has anti-cancer activity in patients with advanced tumors
- Stage
- Phase 1
- Ages
- 18 to 130
- Site
- Research Site, Fairfax, Virginia
- Locations
- 60 in total
- Run by
- AstraZeneca
-
A Study of PHST001 in Advanced Solid Tumors
This is a multi-center, first-in-human (FIH), open-label, Phase 1a/1b dose escalation and dose expansion study to assess the safety, PK, pharmacodynamics, and antitumor activity of PHST001 monotherapy (Phase 1a) or in combination with anticancer therapies (Phase 1b) in adult participants with advan…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Oncology - Virginia, Fairfax, Virginia
- Locations
- 20 in total
- Run by
- Pheast Therapeutics
-
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
- Virginia Cancer Specialists, Fairfax, Virginia
- Locations
- 76 in total
- Run by
- PMV Pharmaceuticals, Inc
-
A Phase 1, First-in-Human (FIH), Open-Label, Dose-Escalation and Dose Expansion Study of the Peptide Drug Conjugate (PDC), TS-104, as a Monotherapy in Subjects With Select Advanced Solid Tumors
A Phase 1, First-in-Human (FIH), Open-Label, Dose-Escalation and Dose Expansion Study of the Peptide Drug Conjugate (PDC), TS-104, as a Monotherapy in Subjects with Select Advanced Solid Tumors. The main goals of this study are to: * Find the recommended dose of TS-104 that can safely be given to p…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Site 04, Fairfax, Virginia
- Locations
- 3 in total
- Run by
- TwoStep Therapeutics, Inc.
-
Evaluate BL-B01D1 in Patients With Metastatic or Unresectable Non-Small Cell Lung Cancer (NSCLC) and Other Solid Tumors
The objective of this study is to evaluate the safety, tolerability, and efficacy of BL-B01D1 in patients with Metastatic or Unresectable Non-Small Cell Lung Cancer (NSCLC) and Other Solid Tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Virginia Cancer Specialists, Fairfax, Virginia
- Locations
- 37 in total
- Run by
- SystImmune Inc.
-
A Study of INCB123667 in Participants With Platinum-Resistant Ovarian Cancer With Cyclin E1 Overexpression
This study will evaluate the safety and efficacy of INCB123667 in Participants With Platinum-Resistant Ovarian Cancer (PROC) With Cyclin E1 Overexpression.
- Stage
- Phase 2
- Ages
- 18 to 99
- Site
- Virginia Cancer Specialists, Fairfax, Virginia
- Locations
- 74 in total
- Run by
- Incyte Corporation
-
FiH Study to Investigate Safety, PK and Efficacy of the NaPi2b ADC TUB-040 in Patients With PROC or r/r Adenocarcinoma NSCLC
The purpose of this multicenter, open label trial (NAPISTAR 1-01) is to evaluate the safety/tolerability, pharmacokinetics and preliminary efficacy of TUB-040 and to find the best dose of TUB-040 in participants with ovarian cancer and Non Small Cell Lung Cancer. TUB-040 is an antibody-drug-conjuga…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Next Oncology Virginia, Fairfax, Virginia
- Locations
- 29 in total
- Run by
- Tubulis GmbH
-
Phase 1 Study to Assess Safety, Tolerability, Pharmacokinetics, Immunogenicity, and Antitumor Activity of ARR-002 in Advanced or Metastatic Ovarian or Endometrial Cancer.
This is a Phase 1 study to assess safety, tolerability, pharmacokinetics, immunogenicity, and antitumor activity of ARR-002 in advanced or metastatic ovarian or endometrial cancer.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Oncology, Fairfax, Virginia
- Locations
- 6 in total
- Run by
- ArriVent BioPharma, Inc.
-
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, Fairfax, Virginia
- Locations
- 18 in total
- Run by
- Normunity AccelCo, Inc.
-
Study Evaluating the Safety and Efficacy of HWK-007, a PTK7-directed Antibody Drug Conjugate in Participants With Advanced Solid Tumors
HWK-007-101 is a multicenter, open-label, first-in-human (FIH) Phase 1 study evaluating HWK-007, a protein tyrosine kinase 7 (PTK7)-targeted antibody drug conjugate (ADC), in adult participants with advanced or metastatic solid tumors known to be expressing PTK7. The study employs a sequential dose…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Oncology - Virginia Cancer Specialists, Fairfax, Virginia
- Locations
- 12 in total
- Run by
- Whitehawk Therapeutics, Inc.
-
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 #112, Fairfax, Virginia
- Locations
- 18 in total
- Run by
- MOMA Therapeutics
-
Relacorilant in Combination With Different Treatment Regimens in Patients With Gynecological Cancers
This is a Phase 2, open-label, global, multi-arm study to evaluate efficacy and safety of relacorilant in combination with other treatments in patients with gynecological cancers.
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- 522, Fairfax, Virginia
- Locations
- 49 in total
- Run by
- Corcept Therapeutics
-
A Study of Emiltatug Ledadotin (Emi-Le) in Participants With Solid Tumors
A Study of Emi-Le in Participants with Solid Tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- NEXT Oncology Virginia, Fairfax, Virginia
- Locations
- 26 in total
- Run by
- Day One Biopharmaceuticals, 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.