[No standalone website (unbranded, no questionnaire)] A Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness of Adalimumab Introduction Compared With Methotrexate Dose Escalation (CONTROL)

How to apply

Determine if a study site for this clinical trial is near you. Contact the study to apply.

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Study’s contact

Call center

617-949-5200

Email address

TC-510@tcr2.com

Condition

Colorectal Cancer,Colorectal Neoplasms,Pancreatic Adenocarcinoma,Pancreatic Cancer,Pancreatic Neoplasms,TNBC - Triple-Negative Breast Cancer,Triple Negative Breast Cancer,Mesothelioma,Mesothelioma Peritoneum,Mesothelioma, Malignant,Mesotheliomas Pleural,Ovarian Adenocarcinoma,Ovarian Cancer,Ovarian Neoplasms,Ovarian Serous Adenocarcinoma

Treatment type

Interventional

Investigational product

TC-510

Phase

Phase 1/Phase 2

Sponsor

TCR2 Therapeutics

ClinicalTrials.gov identifier

NCT05451849

Study number

TCR2-21-01

Understanding clinical trials

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About the study

TC-510 is a novel cell therapy that consists of autologous genetically engineered T cells expressing two synthetic constructs: first, a single-domain antibody that recognizes human Mesothelin, fused to the CD3-epsilon subunit which, upon expression, is incorporated into the endogenous T cell receptor (TCR) complex and second, a PD-1:CD28 switch receptor, which is expressed on the surface of the T cell, independently from the TCR. The PD-1:CD28 switch receptor comprises the PD-1 extracellular domain fused to the CD28 intracellular domain via a transmembrane domain. Thus, the switch is designed to produce a costimulatory signal upon engagement with PD-L1 on cancer cells.

Who can take part?

You may be eligible to participate in the study if you meet the following criteria:

Inclusion criteria

  1. Patient is > 18 years of age at the time the Informed Consent is signed.
  2. Patient has a pathologically confirmed diagnosis of either MPM, Serous Ovarian Adenocarcinoma, Pancreatic Adenocarcinoma, TNBC, and Colorectal Cancer
  3. Patient's tumor has been reviewed with confirmed positive MSLN expression on >/= 50% of tumor cells that are 1+, 2+ and/or 3+ by immunohistochemistry.
  4. Prior to TC-510 infusion, patients must have received at least 1 but no more than 5 systemic therapies for metastatic or unresectable disease with more details provided in the protocol
  5. Patients has an ECOG performance status 0 or 1
  6. Patient is fit for leukapheresis and has adequate venous access for the cell collection.
  7. Patient must have adequate organ function as indicated by the laboratory values in the clinical protocol
Exclusion criteria

  1. Inability to follow the procedures of the study
  2. Known or suspected non-compliance, drug, or alcohol use

For a full list of inclusion/exclusion criteria, please visit ClinicalTrials.gov

Study locations

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How to apply

Determine if a study site for this clinical trial is near you. Contact the study to apply.

Find a Study Site