New drug cocktail aims to beat lymphoma without chemo
NCT ID NCT07496229
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study tests a combination of two drugs, GW5282 and golidocitinib, for people with T-cell lymphoma. The first part finds the safest dose; the second part compares the combo to standard chemotherapy. About 165 adults with newly diagnosed or relapsed disease will take part. The goal is to see if the combo works better and is safer than current treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- GW5282 combined with golidocitinib
- What this could lead to
- If successful, this could offer a new chemo-free combination therapy for T-cell lymphoma, potentially improving response rates and reducing side effects compared to standard treatment.
- What could go wrong
- This is an early phase 1/2 trial with a small number of participants, so results may not apply broadly. The combination may cause unexpected side effects or fail to show better outcomes than standard chemo.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 1/2
Runs two stages together: safety and dose first, then whether the treatment works.
- Participants
-
About 165 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Apr 2026
- Expected to finish
-
Dec 2029
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Signed informed consent; 2. Adult ≥ 18 years of age; 3. ECOG performance status score ≤ 2; 4. Life expectancy of not less than 12 weeks; 5. Histopathologically confirmed diagnosis of PTCL; 6. Presence of measurable disease; 7. Adequate bone marrow function and vital organ function reserve; 8. Ability to comply with study requirements and to complete study-related procedures; 9. Adequate contraception during participation in the trial. Exclusion Criteria: 1. Presence of unresolved drug-related adverse events greater than Grade 1; 2. Lymphoma involving the central nervous system; 3. Failure to complete the required washout period for other anti-tumor therapies; 4. Corticosteroid use that does not meet protocol requirements; 5. Major surgery/trauma within a short period, or planned major surgery within a short period; 6. Vaccination with a live vaccine within a short period; 7. Inability to discontinue prohibited medications; 8. Requirement for immunosuppressive agents or biologics due to an underlying disease; 9. Presence of active infection; 10. Significant cardiovascular disease; 11. Presence of gastrointestinal disease that might affect drug intake or absorption; 12. History of other malignancies; 13. Known allergy to the study drug; 14. Other severe or uncontrolled systemic diseases; 15. Personnel with a conflict of interest (e.g., site staff, sponsor employees); 16. Pregnant or breastfeeding women; 17. Inability to comply with protocol requirements.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Peripheral T-cell lymphoma are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
12 sites. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Chongqing Cancer Hospital
NOT_YET_RECRUITINGChongqing, Chongqing Municipality, China
-
Fudan University Shanghai Cancer Center
RECRUITINGShanghai, China
-
Fujian Cancer Hospital
NOT_YET_RECRUITINGFuzhou, Fujian, China
-
Guangxi Medical University Cancer Hospital
NOT_YET_RECRUITINGNanning, Guangxi, China
-
Henan Cancer Hospital
NOT_YET_RECRUITINGZhengzhou, China
-
Henan Provincial People's Hospital
NOT_YET_RECRUITINGZhengzhou, Henan, China
-
Nanjing Drum Tower Hospital
NOT_YET_RECRUITINGNanjing, Jiangsu, China
-
Shanxi Provincial Cancer Hospital
NOT_YET_RECRUITINGTaiyuan, China
-
Taizhou Hospital of Zhejiang Province
NOT_YET_RECRUITINGTaizhou, Zhejiang, China
-
The First Affiliated Hospital of Wenzhou Medical University
NOT_YET_RECRUITINGWenzhou, Zhejiang, China
-
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
NOT_YET_RECRUITINGWuhan, Hubei, China
-
West China Hospital of Sichuan University
NOT_YET_RECRUITINGChengdu, Sichuan, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can adding linperlisib to standard chemotherapy improve outcomes in rare T-Cell lymphoma?
- Can a powerful combo of drugs and stem cell transplant beat tough lymphomas in kids?
- Can a simple blood test spot lymphoma earlier?
- Can a Five-Drug combo tame a tough lymphoma without standard chemo?
- Can a targeted pill boost Chemotherapy's punch against a rare lymphoma?
- A microchip implanted in tumors could reveal which drugs work best