Cancer drug imatinib tested for rare eye melanoma – but trial stops early
NCT ID NCT00421317
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This phase II trial tested the drug imatinib in 13 adults with metastatic ocular melanoma, a rare eye cancer that has spread. The goal was to see if imatinib could stop tumor growth for at least 3 months. The trial was terminated early, so the results are limited and it is unclear if imatinib helps patients with this condition.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Imatinib
- What this could lead to
- If it works, this could point toward a treatment option for metastatic ocular melanoma, a rare and hard-to-treat cancer.
- What could go wrong
- This trial was terminated early and enrolled only 13 people, so results are very limited. Imatinib may not shrink tumors or improve survival, and it can cause side effects like fatigue, nausea, and liver problems.
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 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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13 people
The number who actually took part.
- Started
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Dec 2005
- Finished
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Nov 2009
- 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
-
18 years and older
- Sex
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Anyone
- Healthy volunteers
-
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: * Metastatic ocular melanoma * Age \> or = 18 years old * Measurable metastases \> or = 10 mm according to RECIST criteria * PS-WHO \< or = 1 or IK \> 70 percent * Normal hepatic function * PNN \> 1500/mm3, platelets \> or = 100 000/mm3 * Contraception * Informed consent signed Exclusion Criteria: * Patient with two prior lines of systemic treatment (chemotherapy, immunotherapy or association) * Other evolutive neoplasic disease * Severe hepatic insufficiency * Severe renal insufficiency * Somatic or psychiatric co-morbidity incompatible with the protocol * Leptomeningeal or cerebral metastatic dissemination * Pregnant or lactating woman * Other antitumoral treatment * Patient participating to another clinical trial with an experimental drug * Known hypersensitivity to Imatinib or one of its excipients * Resecable single metastasis
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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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Centre Francois Baclesse
Caen, 14076, France
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Centre Georges-Francois Leclerc
Dijon, 21079, France
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Centre Gustave Roussy
Villejuif, 94805, France
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Centre Hospitalier Regional Universitaire
Lille, 59035, France
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Centre Jean Perrin
Clermont-Ferrand, 63011, France
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Centre Leon Berard
Lyon, 69373, France
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Centre Oscar Lambret
Lille, 59020, France
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Centre Paul Strauss
Strasbourg, 67065, France
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Centre Val d'Aurelle Paul Lamarque
Montpellier, 34298, France
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Hopital Universitaire de Hautepierre
Strasbourg, 67098, France
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Institut Claudius Regaud
Toulouse, 31052, France
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Institut Curie
Paris, 75248, France
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Other studies related to the condition(s) this trial covers.
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- Can tumor DNA and immune cells reveal why some cancers resist immunotherapy?
- Can a Two-Drug immune combo shrink melanoma tumors?