Status:
NOT_YET_RECRUITING
A Phase 1, Multicenter, Open-label, Prospective, First-in-human Dose-escalation Clinical Trial of Domain Therapeutics' Anti-CCR8 Monoclonal Antibody (DT-7012) in Patients With Relapsed or Refractory Cutaneous T-cell Lymphomas (CTCL)
Lead Sponsor:
Assistance Publique - Hôpitaux de Paris
Collaborating Sponsors:
Domain Therapeutics SA
Conditions:
Cutaneous T Cell Lymphoma (CTCL)
Mycosis Fungoides
Eligibility:
All Genders
18+ years
Phase:
EARLY_PHASE1
Brief Summary
Cutaneous T-cell lymphomas (CTCL) are a heterogeneous group of lymphomas characterized by a primary involvement of the skin. Among them, mycosis fungoides (MF) and Sézary syndrome (SS) are the most co...
Eligibility Criteria
Inclusion
- Adult Patients (≥18 years) with no upper age limit
- Confirmed diagnosis of mycosis fungoides or Sezary syndrome
- Stage IB to IVB in the ISCL / EORTC classification
- Relapsed or refractory (no response) after at least two systemic treatments
- ECOG performance status 0-1
- Adequate liver function:
- Total bilirubin ≤ 1.5 xULN, or Direct bilirubin ≤ 1.5xULN if total bilirubin is \>1.5xULN, or total bilirubin \>1.5 xULN if elevated total bilirubin is attributed to Gilbert's syndrome or to histologically-proven liver involvement by CTCL
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2,5 x ULN, unless elevated to up to 5 x ULN due to CTCL
- Adequate hematological function:
- Absolute neutrophil count of ≥ 1.5 G/L without G-CSF support for at least 7 days
- Platelet count of ≥ 75 G/L without platelet transfusion within 7 days
- Hemoglobin ≥ 9 g/dL without RBC transfusion within 7 days
- Adequate renal function: creatinine clearance calculated by Cockcroft \& Gault formula of ≥ 50 mL/min
- HBV: negative blood HBs Ag or blood HBV DNA. Vaccinated patients may be included. Patients with HBc antibody may be included if HBV DNA is negative
- HCV: negative HCV serology, or negative HCV RNA if HCV serology is positive
- HIV: negative HIV serology
- Negative serum or urinary pregnancy test within 7 days or at baseline prior to study treatment in women of childbearing potential
- Patients must agree to use a highly effective contraceptive method from inclusion until:
- If the patient is a male: at least 6 months after the last dose of DT-7012. Men must refrain from donating sperm during this same period
- If patient is a female of childbearing potential: at least 6 months after the last dose of DT-7012
- Patients must have the following minimum wash-out from previous treatments:
- 12 weeks for total skin electron beam irradiation,
- 4 weeks for monoclonal antibodies
- 3 weeks for local radiation therapy, systemic cytotoxic anticancer therapy, treatment with other anti-neoplastic investigational agents
- 3 weeks for systemic retinoids, interferons, vorinostat, romidepsin, fusion proteins
- 3 weeks for phototherapy
- 2 weeks for topical therapy (including steroids, retinoids, nitrogen mustard or imiquimod). Topical steroids and oral steroids (10 mg prednisone equivalent/day maximum) are allowed, if the patient has been on a stable dose with stable symptoms for at least 4 weeks prior to study entry.
- Patient covered by any social security system (registered or being a beneficiary of such a scheme) for French participants only
- Signed informed consent
Exclusion
- Known central nervous system involvement by CTCL
- Participation in any study of a health product within 30 days prior to study entry
- Patients with a history of other malignancies during the past three years (except for: non-melanoma skin cancer, lymphomatoid papulosis, curatively treated localized prostate cancer, curatively treated localized breast cancer, resected thyroid cancer, biopsy proven cervical intraepithelial neoplasia or cervical carcinoma in situ, which are not considered exclusion criteria).
- Uncontrolled congestive heart failure (New York Heart Association Classification 3 or 4), or angina, myocardial infarction, cerebrovascular accident, transient ischemic attack within 6 months prior to study entry
- Any severe acute or chronic medical or psychiatric condition
- Patients with immunodeficiency
- Any active systemic viral, bacterial, or fungal infection requiring systemic antibiotics within 1 week prior to first study drug dose
- Chronic use of systemic corticosteroids of prednisone or equivalent \>10 mg prednisone equivalent/day for a chronic condition (washout of 8 days from start of treatment is accepted)
- Other immunosuppressive therapies are also excluded, (washout of 7 days from start of treatment is accepted)
- Autologous Hematopoietic Stem Cell Transplantation (HSCT) within 100 days prior to DT-7012 infusion
- Prior allogeneic HSCT
- Prior solid organ transplantation
- Patient with history of confirmed progressive multifocal leukoencephalopathy
- Known or suspected allergies, hypersensitivity, or intolerance to DT-7012 or its excipients
- Pregnant or breast-feeding woman, or desire (for both man and woman participant) to conceive a child within 6 months after end of treatment
- Patient under guardianship or curatorship and protected adults or unable to consent
- Coagulation disorder contra indicating intravenous infusion
- History of anaphylactic reaction following vaccination or immunotherapy
- History or current immune pneumonitis or interstitial lung disease
Key Trial Info
Start Date :
January 1 2026
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 1 2028
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT07213882
Start Date
January 1 2026
End Date
August 1 2028
Last Update
October 9 2025
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