Trials / Not Yet Recruiting
Not Yet RecruitingNCT07032532
Assessing An Oral JAK1 Inhibitor, Golidocitinib, in Patients Who Have Newly Diagnosed Peripheral T-Cell Lymphoma (JACKPOT23)
An Open-Label, Single-Arm, Phase 2 Study to Evaluate the Efficacy and Safety of Golidocitinib in First-Line Therapy of Peripheral T-Cell Lymphoma
- Status
- Not Yet Recruiting
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 35 (estimated)
- Sponsor
- Sun Yat-sen University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study will treat patients with newly diagnosed PTCL, who have no prior systemic treatment for T-cell lymphoma. This study will assess the anti-tumor efficacy of golidocitinib using 2-year Progression-Free Survival rate as primary endpoint. In addition, it will help to understand what type of side effects may occur with the drug treatment.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Golidocitinib | Golidocitinib 150mg orally once daily in a 21-day cycle |
| DRUG | Golidocitinib plus CHOP | Golidocitinib 150mg orally every other day with CHOP (Cyclophosphamide: 750mg/m2, IV, d1 ; Doxorubicin: 50mg/m2, IV, d1; Vincristine: 1.4mg/m2, IV, d1 ; Prednison: 100mg, po, d1-5) in a 21-day cycle for 6 cycles. |
Timeline
- Start date
- 2025-07-01
- Primary completion
- 2028-12-01
- Completion
- 2028-12-01
- First posted
- 2025-06-24
- Last updated
- 2025-06-26
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT07032532. Inclusion in this directory is not an endorsement.