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A Phase 3, Multicenter, Randomized, Open Label Study to Compare the Efficacy and Safety of Golcadomide in Combination with Rituximab (Golca + R) Vs Investigator’s Choice in Participants with Relapsed/Refractory Follicular Lymphoma (GOLSEEK-4)

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-519152-82-00
Acronym
CA073-1003
Enrollment
130
Registered
2025-07-18
Start date
2025-09-03
Completion date
Unknown
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Relapsed/Refractory Follicular Lymphoma

Brief summary

To evaluate time from randomization to the first disease progression based on Lugano 2014 classification guidelines as assessed by Independent Review Adjudication committee (IRAC) or death from any cause, whichever occurs earlier.

Detailed description

To evaluate how long a participant lives overall., To evaluate how well the cancer responds to the treatment., To evaluate how long the cancer responds., To evaluate how long it takes for participants to start a new treatment., To evaluate how the treatment impacts the quality of life of participants while they are taking it.

Interventions

DRUGLENALIDOMIDE
DRUGBENDAMUSTINE HYDROCHLORIDE
DRUGCYCLOPHOSPHAMIDE
DRUGPREDNISOLONE
DRUGVINCRISTINE SULFATE
DRUGPEGFILGRASTIM
DRUGPREDNISONE
DRUGDOXORUBICIN HYDROCHLORIDE
DRUGRITUXIMAB

Sponsors

Celgene Corp.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
To evaluate time from randomization to the first disease progression based on Lugano 2014 classification guidelines as assessed by Independent Review Adjudication committee (IRAC) or death from any cause, whichever occurs earlier.

Secondary

MeasureTime frame
To evaluate how long a participant lives overall., To evaluate how well the cancer responds to the treatment., To evaluate how long the cancer responds., To evaluate how long it takes for participants to start a new treatment., To evaluate how the treatment impacts the quality of life of participants while they are taking it.

Countries

Finland, France, Germany, Greece, Italy, Netherlands, Poland, Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026