Phase 2 Ovarian Cancer Trial, Recruiting NCT04804007 Sponsor: Nabil Adra Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT04804007
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults aged 18 or older at the time of signing consent forms
  • People diagnosed with a non-seminoma germ cell tumour, confirmed through tissue biopsy or blood tests
  • People whose cancer came back after initial treatment with cisplatin-based chemotherapy
  • People who have completed two cycles of high-dose chemotherapy with stem cell transplant as their second-line (salvage) treatment, following the guidelines of the treating institution
  • High-dose chemotherapy must have been the first salvage treatment used, though one or two cycles of certain standard chemotherapy regimens beforehand may be acceptable (confirm with trial site)
  • People whose tumour markers (AFP and hCG blood tests) are normal or falling at the time of screening
  • People whose side effects from previous treatment have mostly resolved to a mild level by the time of registration
  • Women with ovarian germ cell tumours are also eligible
  • People with a general health and activity level rated as reasonably functional (scored 0, 1, or 2 on a standard medical scale), assessed within 28 days of joining the study
  • People whose last high-dose chemotherapy dose was no more than 16 weeks before joining the study
  • People whose blood counts, kidney, liver, and clotting function results fall within the required ranges, tested within 28 days before joining the study
  • Women who could become pregnant must have a negative pregnancy test within 28 days before starting the study treatment
  • Participants who are able to use two highly effective forms of contraception from the first dose of study treatment until 30 days after the last dose, or who abstain from heterosexual activity during that period

Who may not be able to join:

  • People with a pure seminoma type of germ cell tumour that has relapsed
  • People whose tumour markers (AFP and hCG) are rising at the time of screening
  • People whose last high-dose chemotherapy dose was more than 16 weeks before the study registration date
  • People who have received any other experimental treatment within 28 days before joining the study
  • People who have had another active cancer requiring treatment in the past 12 months
  • People with a history of psychiatric illness or personal circumstances that could make it difficult to follow the study requirements
  • People with an active infection that requires treatment with antibiotics, antifungals, or other systemic medicines
  • People who have previously had a serious allergic reaction to etoposide that did not improve with supportive care
  • People who are pregnant, breastfeeding, or currently lactating
  • People whose overall health, other medical conditions, or test results may interfere with the study results or make participation not in their best interest, as determined by the treating doctor

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
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.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Nabil Adra, MD, Indiana University

Phone: 317-274-5830

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Nabil Adra
Registry
ClinicalTrials.gov
Start date
3 March 2021
Est. completion
1 December 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

12-month Progression Free Survival

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov