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First-in-human Trial of STC-1010, an Immunotherapy, in Patients With Unresectable Locally Advanced or Metastatic Colorectal Cancer

RecruitingPhase 1, Phase 2Ages 18 Years - 75 YearsAllBrenus Pharma
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In plain words

What the trial is, and whether it could suit you

This is a phase I/IIA, first-in-human (FIH), two-part, open-label, multicenter study to characterize the safety, tolerability profile, and clinical efficacy of STC-1010 associated with GM-CSF and cyclophosphamide immunostimulant (IS) regimen administered with standard of care (SOC) therapy (mFOLFOX6 with or without bevacizumab) to participants with unresectable locally advanced (stage IIIC, T4b) or unresectable metastatic (stage IV) colorectal cancer (CRC). The trial will be conducted in two parts: * A Phase I consisting of a dose escalation part and small expansion part to determine the maximum tolerated dose (MTD), recommended Phase II dose (RP2D) and safety profile of the STC-1010 + IS regimen administered with SOC therapy. Approximately 21 to 33 participants will be included in this phase in Europe. * A Phase IIA consisting of the expansion stage of the study which will further eva

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📋 Eligibility rules (as published)
Inclusion Criteria: 1. Male or female aged 18-75 years 2. Histologically confirmed diagnosis of unresectable locally advanced (stage IIIC, T4b) or unresectable metastatic (stage IV) (R0) adenocarcinoma of the colon or rectum 3. Adjuvant fluoropyrimidine monotherapy or oxaliplatin-based chemotherapy allowed if more than 6 months have elapsed between the end of adjuvant treatment and first relapse 4. Determination of KRAS and BRAF mutation status 5. Measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST 1.1) 6. Must agree to have biopsy at screening and on-treatment, only if not representing an unacceptable clinical risk and/or if technically feasible as judged by the Investigator in discussion with the interventional radiologist or endoscopist 7. Eastern Cooperative Oncology Group (ECOG) performance status (PS) ≤ 1. Participants \>70 years must have a PS= 0. 8. Life expectancy \> 3 months as assessed by the investigator 9. Effective contraceptive measures implemented Exclusion Criteria: 1. Patients with symptomatic ascites or pleural effusion 2. Dihydropyrimidine dehydrogenase (DPD) deficiency 3. Resectable tumor with curative intent or patient considered for a curative strategy by intensifying chemotherapy to induce resectability 4. Prior chemotherapy for metastatic disease 5. Prior immunotherapy for advanced/metastatic disease (except for Arm 2A-2) 6. Prior therapy with an investigational agent 7. BRAF mutation 8. Active auto-immune diseases such as rheumatoid arthritis, lupus, Crohn's disease, ulcerative colitis 9. Medical conditions requiring immunosuppressive therapy 10. Major surgery \<4 weeks prior to first administration of STC-1010 11. Radiotherapy \< 4 weeks prior to first administration of STC-1010 or \< 2 weeks in case of palliative radiotherapy 12. Prior stem cell or solid organ transplantation 13. Dementia or altered mental status or subject of a legal protection measure that would prohibit informed consent 14. Active drug or alcohol abuse as assessed by the Investigator 15. Participant deprived of their liberty by a judicial or administrative decision, undergoing psychiatric care and admitted to a health or social establishment for purposes other than research.
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What it tests

  • STC-1010 + IS regimen + SOC therapy
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Where

9 sites
Johns Hopkins
Baltimore, United States
Institut Jules Bordet
Brussels, Belgium
Institut Bergonié
Bordeaux, France
Centre Georges François Leclerc (CGFL)
Dijon, France
Centre Léon Bérard (CLB)
Lyon, France
Hospices Civils de Lyon (HCL)
Lyon, France
Institut du Cancer de Montpellier (ICM)
Montpellier, France
Centre Hospitalier Universitaire de Poitiers (CHU)
Poitiers, France

…and 1 more on ClinicalTrials.gov.

🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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