OTHERClinicalTrials.govClinical trialPhase 3Recruiting
Modified DHAP Versus Standard DHAP in Relapsed/Refractory Diffused Large B-cell Lymphoma.
Official record
- Identifier
NCT07739654- Recruiting locations
country
Pakistan- Interventions studied
- CisplatinCisplatin
- Lead sponsor
- King Edward Medical University
- Target enrolment
- 74 participants
- Study type
- INTERVENTIONAL
- Phase
- Phase 3
- Status
- Recruiting
- First posted
- Jul 31, 2026
- Last updated on the registry
- Jul 31, 2026
- Age
- 18 Years
- Sex
- ALL
- Study contact
- The official record lists a study contact. Contact details are published there and are intentionally not copied to this page.
- Eligibility criteria
Reproduced verbatim from the official record. Eligibility is decided by the study team, never by this page.
Inclusion Criteria: * Histologically confirmed relapsed or refractory DLBCL * Adults ≥ 18 years * At least one prior line of therapy for lymphoma * ECOG performance status 0-2 * Ability to provide informed consent and comply with study requirements * Adequate organ function: * Hematologic: ANC ≥ 1,000 cells/mm³, Platelets ≥ 75,000 cells/mm³ * Renal: Serum creatinine ≤ 1.5 × ULN * Hepatic: Total bilirubin ≤ 1.5 × ULN, AST/ALT ≤ 2.5 × ULN (if no liver metastases) Exclusion Criteria: * History of other malignancies within last 5 years (except non-melanoma skin cancer or localized prostate cancer) * Pregnant or breastfeeding women * Significant uncontrolled medical conditions (e.g., cardiovascular disease, uncontrolled diabetes) * Receipt of investigational agents within 30 days prior to enrollment * Known severe allergic reactions to DHAP components (dexamethasone, cytarabine, cisplatin) * Concurrent anti-cancer treatments (chemotherapy, radiotherapy) during study period
- Indexed under
- Lymphoma
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