Daily Low-Dose chemo tested for patients with no other options
NCT ID NCT00420563
First seen Jun 24, 2026 · Last updated Sep 18, 2026 · Updated 3 times
Summary
This study tested two treatments for people with advanced cancer who cannot have standard therapy. One group took a low-dose chemotherapy pill (cyclophosphamide) daily, and the other took a hormone pill (megestrol). The goal was to see which treatment could slow cancer growth for at least two months. The trial enrolled 88 adults with various cancers (except breast cancer) and measured how long the cancer stayed under control.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- cyclophosphamide (low-dose chemotherapy) and megestrol (hormone therapy)
- What this could lead to
- If successful, this could offer a gentle, long-term chemotherapy option for patients with advanced cancer who have run out of standard treatments.
- What could go wrong
- This is a small, early-phase trial with only 88 participants. The benefit may be modest, and side effects like low blood counts or blood clots are possible.
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
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
88 people
The number who actually took part.
- Started
-
Sep 2009
- Finished
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Jan 2011
- Lead sponsor
-
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
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age \> or = 18 * PS-WHO \< or = 1 * Histologically proven cancer * No other therapeutic proposal * Treatment can be orally taken * Radiologic proof of evolutive character of the disease * Effective contraception Exclusion Criteria: * Hypercalcemia ( Ca \> 2.65 mmol/l) * Breast cancer * Thrombosis or pulmonary embolism * Dysphagia, malabsorption * Polynuclear neutrophil leukocytes \< 1000/mm3 * Treatment with Tegretol * Active and uncontrolled infection * Evolutive psychiatric disease * Pregnant or lactating woman
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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
-
Centre Hospitalier Regional - Dermatology
Lille, 59035, France
-
Centre Hospitalier Regional - Oncology
Lille, 59035, France
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Centre Oscar Lambret
Lille, 59020, France
-
Hopital Saint Vincent
Lille, 59020, France
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