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NCT02489903
NCT02489903
Who may be able to join
Who might be able to join this trial:
- You have been diagnosed with one of the following advanced or spreading cancers, confirmed by a lab test: small cell carcinoma (at least 3rd line treatment or platinum-resistant/refractory in 2nd line), a specific type of non-small cell lung cancer with an EGFR mutation (after prior platinum and targeted therapy), certain ovarian, fallopian tube, or related cancers (after prior platinum treatment or with platinum-resistant disease), or a high-grade neuroendocrine carcinoma from any part of the body (after prior chemotherapy).
- Your cancer can be measured on a scan using standard guidelines (RECIST v1.1).
- It has been at least 3 weeks since your last cancer treatment.
- You have previously received a platinum-based chemotherapy for your advanced cancer and either did not respond or relapsed within 6 months.
- You are 18 years of age or older.
- Doctors expect you to live for at least 12 weeks or more.
- You are reasonably well and able to carry out daily activities (confirm with trial site — this is measured using a standard scale called ECOG 0–2).
- Your blood counts, kidney function, and liver function meet certain minimum levels before starting treatment (confirm with trial site for specific numbers).
- You agree to allow the trial team and sponsor to access your past medical records, previous scans, and any stored tumor tissue samples.
- You are able to understand and sign a consent form agreeing to take part.
- If you are a woman who could become pregnant, or a man whose partner could become pregnant, you must agree to use reliable contraception during the trial and for 90 days after finishing treatment.
Who may not be able to join:
- You are currently taking part in another clinical trial involving an experimental treatment.
- You have cancer that has spread to the brain and is causing symptoms (for example, if you need increasing doses of steroids to manage them).
- You previously had to permanently stop platinum-based chemotherapy because of serious side effects (such as kidney damage, hearing loss, or severe nerve damage).
- You have had a severe allergic reaction to platinum-based drugs (such as carboplatin or cisplatin) or to certain chemotherapy drugs that are used alongside platinum in this trial.
- You have a serious ongoing medical condition that doctors feel would make it too risky for you to participate, such as uncontrolled diabetes, significant heart failure, a heart attack in the past 6 months, severe lung disease, uncontrolled infection, or uncontrolled fluid build-up in the lungs.
- You are pregnant or currently breastfeeding.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Trial details
Status
Completed
Phase
Phase 2
Sponsor
EpicentRx, Inc.
Registry
clinicaltrials_gov
Start date
1 June 2015
Est. completion
6 December 2021
Where this trial is recruiting
🇺🇸 United States
Primary endpoints
Overall Survival
Can't join this trial?
Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.