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NCT05284825

A Phase II Trial of Intermediate Radiation Dose For Lymphoma

Status unknown NA Last updated 15 February 2024
What this trial tests

NA trial testing 12 Gy in 6 daily fractions in Follicular Lymphoma in 27 participants. Status unknown.

Timeline
28 February 2022
Primary endpoint
1 January 2025
1 January 2025

Quick facts

Lead sponsorSunnybrook Health Sciences Centre
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment27
Start date28 February 2022
Primary completion1 January 2025
Estimated completion1 January 2025
Sites1 location across Canada

Drugs / interventions tested

Conditions studied

Sponsor

Sunnybrook Health Sciences Centre — full company profile →

Who can join

18 and older, any sex, with Follicular Lymphoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to determine the optimal radiation dose fractionation regimen for low grade follicular lymphoma. It is hypothesized that the complete response rate with the use of 12 Gy in 6 daily fractions is 80% (10% total width of the confidence interval) at 3 months. This phase II study will evaluate whether an intermediate dose for follicular lymphoma is associated with excellent response rates while minimizing acute and late toxicity.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Follicular Lymphoma

Currently open trials in the same condition.

Other Sunnybrook Health Sciences Centre trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05284825.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing