CT-95 in Advanced Cancers Associated With Mesothelin Expression

Part of paid clinical trials in Denver, Colorado.

Sponsor
Context Therapeutics Inc.
Study ID
NCT06756035
Phase
PHASE1
Status
Recruiting

Conditions

  • Cholangiocarcinoma Advanced
  • Cholangiocarcinoma Non-resectable
  • Colorectal Cancer
  • Epithelial Ovarian Cancer
  • Lung Adenocarcinoma Metastatic
  • Malignant Peritoneal Mesothelioma, Advanced
  • Malignant Pleural Mesothelioma, Advanced
  • Mesothelin-Expressing Tumors
  • Mesothelin-expressing Advanced Cancers
  • Mesothelin-positive Advanced Malignant Solid Tumors
  • Pancreatic Adenocarcinoma Advanced or Metastatic

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • CT-95 — DRUG
    Weekly IV dosing

Study Details

This is a Phase 1a/1b open-label, dose escalation study to evaluate the safety and efficacy of CT-95 (study drug), a humanized T cell engaging bispecific antibody targeting Mesothelin, in subjects with advanced solid tumors associated with Mesothelin expression.

Key Dates

Start date
Mar 31, 2025
Status verified
Jun 2026
Primary completion
Dec 31, 2026
Completion
Dec 31, 2028

Study Design

Enrollment
70 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: CT-95
    Each dose cohort will have weekly dosing. Anticipate approximately 8 dose cohorts.

Primary Outcome Measure

Determine the MTD or RD of CT-95 [Safety and Tolerability] [ Time Frame: From date of first dose of CT-95 until 28 days following the first dose. ]

Central Contacts

Locations (9)

FacilityCityStateZIPSite coordinators
Context Investigational SiteDenverColorado80218
Front Desk
720-754-2610
Context Investigational SiteChicagoIllinois60637
Cancer Clinical Trials
773-702-6233
Context Investigational SiteGrand RapidsMichigan49546
Ashley Spagnuolo
616-954-5552
Context Investigational SiteHackensackNew Jersey07601
Oncology Clinical Research Referral Office
551-996-1777
Context Investigational SitePhiladelphiaPennsylvania19107
Ask Phase1
215-586-0199
University of PennsylvaniaPhiladelphiaPennsylvania19104
Andrea Standish
215-662-2419
Context Investigational SiteNashvilleTennessee37203
Sarah Cannon Research Institute
844-482-4812
Context Investigational SiteSan AntonioTexas78229
Clinical Trial Navigator
210-580-9521
Context Investigational SiteSan AntonioTexas78229
Isabel Jimenez
210-593-5265
Christina Santana

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