Ireland
--:--IST
Latest
Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact
Active, not recruiting Phase 1/2

First-in-Human Study of ICT01 in Patients With Advanced Cancer

NCT04243499 · tracked via the Priya Life Science France tracker
Sponsor
ImCheck Therapeutics, an Ipsen company
Phase
Phase 1/2
Started
2020-03-05
Last updated
2026-09-04

Condition(s) studied

Solid Tumor, AdultHematopoietic/Lymphoid Cancer

Investigational drug(s) / intervention(s)

IV ICT01

IV ICT01: humanized anti-Butyrophilin 3A (BTN3A) monoclonal antibody

Study summary

Part 1 will be a dose escalation study of IV ICT01 (a monoclonal antibody targeting BTN3A) as monotherapy in patients with advanced solid or hematologic tumors, followed by a cohort examining the combination of ICT01 plus pembrolizumab (Keytruda). Part 2 will be a cohort expansion into 2 solid tumor indications and one hematologic malignancy for ICT01 monotherapy, and 3 solid tumor indications for the combination of ICT01 plus pembrolizumab.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Voluntarily signed informed consent form. 2. Relapsed/refractory patients with histologically or cytologically confirmed diagnosis of advanced-stage or recurrent cancer, including: Group A: bladder, breast, colon, gastric, melanoma, ovarian, prostate and PDAC Group B: hematologic malignancies including acute myeloid leukemia, acute lymphocytic leukemia, Diffuse large B cell lymphoma and follicular lymphoma Group C: melanoma, cervical, bladder, gastric, head and neck SCC, and lymphoma (according to the approved package labeling of the ICI) Part 2, Group D: Ovarian cancer (2L/3L) with baseline g9d2 T cells \> 20K Part 2, Group E: metastatic castrate resistant prostate cancer (2L/3L) with baseline g9d2 T cells \> 20K Part 2, Group F: newly diagnosed AML starting venetoclax/azacitidine Part 2, Group G: checkpoint-refractory metastatic melanoma with g9d2 T cells \>5K Part 2, Group H: chemotx-refractory or Pt-ineligible urotherlial cancer (bladder) with g9d2 T cells \>5K Part 2, Group I: checkpoint-refractory, metastatic HNSCC with g9d2 T cells \>5K 3. Eastern Cooperative Oncology Group (ECOG) performance status ≤ 1 4. Life expectancy \> 3 months as assessed by the Investigator 5. At least 1 measurable lesion per Response Evaluation Criteria in Solid Tumors (RECIST)/ Response Evaluation Criteria in Lymphoma (RECIL) or \>5% marrow blasts Exclusion Criteria: 1. Any malignancy of Vγ9Vδ2 T cell origin 2. Any anti-tumor-directed drug therapy within 28 days or 5 times the elimination half-life (whichever is shorter) before study treatment (does not apply to patients receiving ICI for the combination arm) 3. Treatment with investigational drug(s) within 28 days before study treatment 4. Systemic steroids at a daily dose of \> 10 mg of prednisone, \> 2 mg of dexamethasone or equivalent, for the last 28 days and need for ongoing treatment. 5. Patients with rapidly progressing disease defined as advanced/metastatic, symptomatic, visceral spread, with a risk of life-threatening complications in the short term (e.g., during Screening Period/ treatment washout) that includes patients with massive uncontrolled effusions pleural, pericardial, peritoneal, pulmonary lymphangitis, and over 50% liver involvement 6. Ongoing immune-related adverse events (irAEs) and/or AEs ≥grade 2 not resolved from previous therapies except vitiligo, stable neuropathy up to grade 2, hair loss, and stable endocrinopathies with replacement hormone therapy. 7. Within 4 weeks of major surgery 8. Documented history of active autoimmune disorders requiring systemic immunosuppressive therapy within the last 12 months 9. Primary or secondary immune deficiency 10. Active and uncontrolled infections requiring intravenous antibiotic or antiviral treatment

Primary outcome measure(s)

  • Percentage of participants with TEAES (Part 1) — From baseline to at least 6 months
    Treatment emergent adverse events (TEAEs) with severity according to National Cancer Institute \[NCI\]- Common Terminology Criteria for Adverse Events \[CTCAE\] Version 5.0.
  • Percentage of participants with TEAES leading to discontinuation of study treatment or treatment modifications (Part 1) — From baseline to at least 6 months
    Treatment emergent adverse events (TEAEs) with severity according to National Cancer Institute \[NCI\]- Common Terminology Criteria for Adverse Events \[CTCAE\] Version 5.0.
  • Percentage of participants with SAEs (Part 1) — From baseline to at least 6 months
    Serious Adverse Events (SAEs) with severity according to National Cancer Institute \[NCI\]- Common Terminology Criteria for Adverse Events \[CTCAE\] Version 5.0
  • Percentage of participants with clinically significant change from baseline clinical laboratory abnormalities (Part 1) — From baseline to at least 6 months
    With severity measured according to NCI-CTCAE Version 5.0
  • Percentage of participants with clinically significant change from baseline vital sign readings (Part 1) — From baseline to at least 6 months
    Vital signs will be assessed by the investigators for clinical significance.
  • Percentage of participants with clinically significant change from baseline in 12-lead Electrocardiogram (ECG) readings (Part 1) — From baseline to at least 6 months
    12-lead (echocardiogram) ECGs will be assessed by the investigators for clinical significance.
  • Percentage of participants with clinically significant change from baseline physical examinations (Part 1) — From baseline to at least 6 months
    Physical examinations will be assessed by the investigators for clinical significance.
  • Duration of Complete Response (DCR) (Part 2) — From baseline to at least 6 months
    DCR according to RECIST Version 1.1 for all groups except Group F (complete response \[CR\] + partial response \[PR\] + stable disease \[SD\]);

Trial sites (29)

FacilityCityRegionStatus
Banner MD Anderson Cancer Center Gilbert Arizona
City of Hope Comprehensive Cancer Center Duarte California
Yale Cancer Center New Haven Connecticut
H. Lee Moffitt Cancer Center and Research Institute Tampa Florida
Montefiore Medical Center The Bronx New York
The University of Texas MD Anderson Cancer Center Houston Texas
US Oncology Research Irving Texas
University of Washington Seattle Washington
Institut Jules Bordet Brussels Belgium
Institut Bergonie Bordeaux France
Haut Leveque Bordeaux France
Centre Hospitalier Lyon Sud Lyon France
Centre Lyon Berard Lyon France
CHU Lyon Lyon France
Institut Paoli-Calmettes Marseille France
CHU Nantes Nantes France
Centre Antoine Lacassagne Nice France
Pitie-Salpetriere Paris France
Institut Curie Paris France
Gustave Roussy Paris France
CHU Poitiers Poitiers France
University Carl Gustav Carus Clinical Trial Unit Dresden Germany
universitatklinikum Wurburg Würzburg Germany
START Barcelone HM Nou Delfos Barcelona Spain
Vall d'Hebron Instiute of Oncology Barcelona Spain
START Madrid-FJD, Hospital Fundación Jiménez Díaz Madrid Spain
Hospital Universitario HM Sanchinarro Madrid Spain
NHS Greater Glasgow and Clyde, Beatson West of Scotland Cancer Centre Glasgow United Kingdom
Institute of Cancer Research London United Kingdom
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04243499 on ClinicalTrials.gov ↗ ← All trials in France