Advanced Solid Tumor Clinical Trials in Philadelphia, Pennsylvania
22 studies are recruiting for advanced solid tumor 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.
Search these by distance from you
Studies now recruiting
-
Study of ISM6331 in Participants With Advanced/Metastatic Mesothelioma or Other Advanced Solid Tumors
This is a Phase 1/2, open-label, multicenter, FIH study to evaluate the safety, tolerability, recommended Phase 2 dose (RP2D), PK/PD, and preliminary anti-tumor activity of ISM6331 in participants with advanced or metastatic mesothelioma or other Advanced solid tumors. The study consists of two par…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Pennsylvania - Abramson Cancer Center, Philadelphia, Pennsylvania
- Locations
- 10 in total
- Run by
- InSilico Medicine Hong Kong Limited
-
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
- 77 in total
- Run by
- PMV Pharmaceuticals, Inc
-
Study of ART6043 in Advanced/Metastatic Solid Tumors Patients (POLKA)
This interventional study will evaluate the safety, tolerability, pharmacokinetics, and preliminary efficacy of ART6043 as monotherapy or in combination with olaparib.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Jefferson University Hospitals - Kimmel Cancer Center, Philadelphia, Pennsylvania
- Locations
- 18 in total
- Run by
- Artios Pharma Ltd
-
An Investigational Study of BGB-58067 As a Single Agent and in Combination With Anticancer Agents in Participants With Advanced Solid Tumors
This is an open-label, multicenter, first-in-human dose escalation and dose expansion study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary antitumor activity of BGB-58067 alone, in combination with BG-89894 (discontinued), and in combination with standard …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sidney Kimmel Cancer Center, Philadelphia, Pennsylvania
- Locations
- 101 in total
- Run by
- BeOne Medicines
-
Safety, Pharmacokinetics (PK), and Efficacy of ONC-783 in Advanced Solid Tumors
ONC-783-001 is a Phase I open label, dose-escalation study for evaluating the safety, pharmacokinetics (PK) and efficacy of ONC-783 as a single agent in patients with advanced/metastatic solid tumors, focusing on colorectal cancer, ovarian cancer, pancreatic cancer, or breast cancer.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Pennsylvania Abramson Cancer Center, Philadelphia, Pennsylvania
- Locations
- 3 in total
- Run by
- OncoC4, Inc.
-
Study of Lunresertib Alone or in Combination With RP-3500 or Debio 0123 in Patients With Advanced Solid Tumors
The primary purpose of this study is to assess the safety and tolerability of lunresertib alone and in combination with RP-3500 or in combination with Debio 0123 in patients with eligible advanced solid tumors, determine the maximum tolerated dose (MTD) and assess preliminary anti-tumor activity.
- Stage
- Phase 1
- Ages
- 12 and older
- Site
- #1010, University of Pennsylvania, Philadelphia, Pennsylvania
- Locations
- 26 in total
- Run by
- Debiopharm International SA
-
A Study of BGB-B455 in Adults With Advanced or Metastatic Solid Tumors
The goal of this clinical trial is to learn if BGB-B455 can treat advanced or metastatic solid tumors expressing claudin 6 (CLDN6), a protein that is found on some tumors. The main questions it aims to answer are: * What is the recommended dosing for BGB-B455? * What medical problems do participant…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sidney Kimmel Cancer Center, Philadelphia, Pennsylvania
- Locations
- 11 in total
- Run by
- BeOne Medicines
-
A Study of Tulmimetostat DZR123 (CPI-0209) in Patients With Advanced Solid Tumors and Lymphomas
The purpose of this open-label, first-in-human (FIH) trial is to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary antitumor activity of DZR123 (Tulmimetostat, CPI-0209), both as monotherapy and in combination with enzalutamide, in patients with advanced solid t…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Abramson Cancer Center of the University of Pennsylvania, Philadelphia, Pennsylvania
- Locations
- 80 in total
- Run by
- Novartis Pharmaceuticals
-
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
-
Study of STK-012 Alone and With Other Treatments in Patients With Advanced Lung Cancer and Other Cancers
This is a phase 1/2, multicenter, open-label study. The phase 1 portion is a dose escalation and expansion study of STK-012 as monotherapy and in combination therapy in patients with selected advanced solid tumors. The phase 2 portion is a randomized study of STK-012 in combination with standard of…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Fox Chase Cancer Center, Philadelphia, Pennsylvania
- Locations
- 47 in total
- Run by
- Synthekine
-
A Study of PYX-201 in Advanced Solid Tumors
The primary objectives of this study are to determine the recommended dose(s) of PYX-201 for participants with recurrent/metastatic (R/M) solid tumors, and to determine the objective response rate (ORR) in participants treated with PYX-201 as a single agent.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Pennsylvania, Abramson Cancer Center, Philadelphia, Pennsylvania
- Locations
- 29 in total
- Run by
- Pyxis Oncology, Inc
-
SNV1521 in Participants With Advanced Solid Tumors
This study is testing a new medicine, SNV1521, for people with advanced cancers. The researchers want to find out if SNV1521 is safe, well-tolerated, and effective in treating solid tumors. They are investigating different doses in order to find the most effective and safe one. They are also invest…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Thomas Jefferson University, Philadelphia, Pennsylvania
- Locations
- 25 in total
- Run by
- Synnovation Therapeutics, Inc.
-
Safety, Pharmacokinetics (PK), and Efficacy of ONC 841 in Advanced Solid Tumors
This is a Phase I/II open label study of intravenous (IV) infusion of ONC-841 as a single agent or in combination in patients with advanced/metastatic solid tumors. The study will evaluate seven dose levels of ONC-841. The Phase 1 part is dose escalation with 7 dose levels of ONC-841 and the dose e…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Thomas Jefferson University Hospital, Philadelphia, Pennsylvania
- Locations
- 8 in total
- Run by
- OncoC4, Inc.
-
Study of Ifinatamab Deruxtecan (DS-7300a, I-DXd) in Participants With Advanced Solid Malignant Tumors
This is a single group study of participants with advanced solid tumors who have not been cured by other treatments. It is the first time the drug will be used in humans, and will be in two parts. The primary purpose of the parts are: * Dose Escalation Part: To evaluate the safety and tolerability …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sidney Kimmel Cancer Center - Thomas Jefferson, Philadelphia, Pennsylvania
- Locations
- 28 in total
- Run by
- Daiichi Sankyo
-
A Study to Evaluate PEEL-224 in Patients With Advanced Solid Tumors
This is a first-in-human, dose escalation, repeat-dose, multi-center, open-label study evaluating safety, tolerability, PK, and preliminary antitumor activity of PEEL-224 in patients with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Abramson Cancer Center at Pennsylvania Hospital, Philadelphia, Pennsylvania
- Locations
- 8 in total
- Run by
- Peel Therapeutics Inc
-
A Study With NKT3964 for Adults With Advanced/Metastatic Solid Tumors
The goal of the Dose Escalation phase 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. The goal of the Expa…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sidney Kimmell Cancer Center - Jefferson Health, Philadelphia, Pennsylvania
- Locations
- 19 in total
- Run by
- NiKang Therapeutics, Inc.
-
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.
-
JZP898 Intravenous Infusion as Monotherapy and Combination With Pembrolizumab in Adults With Advanced/Metastatic Solid Tumors
This Phase 1 first-in-human study will investigate the safety, tolerability, pharmacokinetics (PK), immunogenicity, and preliminary antitumor activity of JZP898 monotherapy as well as JZP898 in combination with pembrolizumab in adult participants with advanced or metastatic solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sidney Kimmel Cancer Center at Thomas Jefferson University Hospital, Philadelphia, Pennsylvania
- Locations
- 10 in total
- Run by
- Jazz Pharmaceuticals
-
FT825/ONO-8250, an Off-the-Shelf, HER2 CAR-T, With or Without Monoclonal Antibodies in Advanced Solid Tumors
This is a phase 1 study designed to evaluate the safety, tolerability, and antitumor activity of FT825 (also known as ONO-8250) with or without monoclonal antibody therapy following chemotherapy in participants with advanced human epidermal growth factor receptor 2 (HER2)-positive or other advanced…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Thomas Jefferson University, Sidney Kimmel Cancer Center, Philadelphia, Pennsylvania
- Locations
- 14 in total
- Run by
- Fate Therapeutics
-
Study of AVZO-021 in Patients With Advanced Solid Tumors
This study, the first clinical trial of AVZO-021, aims to determine the safety, tolerability, pharmacokinetics, pharmacodynamics, maximum tolerated dose, and anti-tumor effects of AVZO-021 in patients with advanced solid tumors. AVZO-021 is an oral medication that inhibits cyclin-dependent kinase 2…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sidney Kimmel Cancer Center (SKCC) at Jefferson Health, Philadelphia, Pennsylvania
- Locations
- 13 in total
- Run by
- Avenzo Therapeutics, Inc.
-
A Phase I Safety and Pharmacokinetic Study of Gamitrinib Administered Intravenously to Patients With Advanced Cancer
This is a first-in-human, phase I, open-label, non-randomized dose-escalation and dose-expansion study with the primary objective to determine the safety profile of small molecule, mitochondrial-targeted Hsp90 inhibitor, gamitrinib, including identification of dose-limiting toxicities (DLT) and max…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Fox Chase Cancer Center, Philadelphia, Pennsylvania
- Run by
- Fox Chase Cancer Center
-
A Study to Evaluate Tovorafenib in Pediatric and Young Adult Participants With Relapsed or Progressive Low-Grade Glioma and Advance Solid Tumors
This is a Phase 2, multi center, open-label study to evaluate the safety and efficacy of Type II RAF (tovorafenib) in pediatric participants with low-grade glioma or advanced solid tumors. Qualifying genomic alterations will be identified through molecular assays as routinely performed at Clinical …
- Stage
- Phase 2
- Ages
- 0 to 25
- Site
- Children's Hospital of Philadelphia, Philadelphia, Pennsylvania
- Locations
- 35 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.