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Clinical Trials/CTRI/2020/10/028220
CTRI/2020/10/028220RecruitingPhase 2

A phase II randomized study to evaluate the efficacy of short-course RR CVEP regimen against short course EPOCH-RR in adolescent and adult seropositive Diffuse large B cell lymphoma.

Tata Memorial Hospital Research Administrative Council0 sites0 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
Phase 2
Status
Recruiting
Sponsor

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • 1. Patients with histologically proven AIDS related diffuse large B cell lymphoma (excluding Burkittââ?¬•s or Burkittââ?¬•s-like lymphomas) with or without CNS involvement
  • 2. No prior chemotherapy for lymphoma
  • 3. Absolute CD4 count >50/Ã?µL.
  • 4. Age- 15-65 years
  • 5. ECOG Performance status <4
  • 6. Adequate organ function
  • 7. Written informed consent
  • 8. Able to comply with the study protocol- absence of psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule

Exclusion Criteria

  • 1.Presence of other co-morbidities (e.g. uncontrolled diabetes mellitus, uncontrolled hypertension, cerebrovascular event in last 6 months, myocardial infarction within last 6 months, uncontrolled arrhythmias, congestive heart failure, other conditions) which can result in poor tolerance to therapy in investigators opinion.
  • 2. Ongoing uncontrolled infections
  • 3. Primary CNS lymphoma
  • 4. Pregnancy
  • 5. Patients on anti-tubercular therapy or other enzyme inducer drugs.

Investigators

Sponsor
Tata Memorial Hospital Research Administrative Council

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