Head-to-Head chemo battle: which regimen works better for hodgkin lymphoma?
NCT ID NCT07450508
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This Phase 3 trial tested two chemotherapy combinations—BEGEV and GDP—in 88 adults with relapsed or refractory classical Hodgkin lymphoma. Patients received either regimen in 21-day cycles, and their response was checked with a PET scan after three cycles. Those who achieved at least a partial response went on to high-dose chemo and stem cell rescue. The study aimed to see which regimen had a better overall response rate and longer disease control.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- BEGEV (bendamustine, gemcitabine, vinorelbine) and GDP (gemcitabine, dexamethasone, cisplatin)
- What this could lead to
- If BEGEV works better than GDP, it could offer a more effective chemotherapy option for people whose Hodgkin lymphoma has come back or not responded to initial treatment.
- What could go wrong
- This is a completed Phase 3 trial with 88 participants, so results are more reliable than early-phase studies. However, both regimens are chemotherapies with significant side effects, and the trial does not test a cure—patients still need high-dose chemo and stem cell rescue afterward.
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
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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88 people
The number who actually took part.
- Started
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Apr 2024
- Finished
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Feb 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 70 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Primary refractory classical Hodgkin lymphoma Relapsed classical Hodgkin lymphoma Age 18 years old or more Both genders Eligible to receive the chemotherapeutic protocol. Exclusion Criteria: Eastern Cooperative Oncology Group(ECOG) performance status less than 2. Pregnancy. Second cancers. Chronic kidney disease End stage renal disease Liver cell failure HIV HCV HBV Autoimmune diseases
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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.
Contacts and locations
Locations
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National Cancer Institute
Cairo, From Elkhart, 11796, Egypt