Phase 3 Lymphoma Trial, Terminated NCT01732926 Sponsor: Gilead Sciences Condition: Lymphoma
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Trial results

AI generated results 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

According to the results reported on ClinicalTrials.gov, this trial enrolled 475 people with a type of slow-growing blood cancer called indolent non-Hodgkin lymphoma. Participants were divided into two groups: 320 people received idelalisib combined with two chemotherapy medicines (bendamustine and rituximab), while 155 people received a placebo (an inactive dummy treatment) combined with the same two chemotherapy medicines. The trial was measuring how long people went without their cancer getting worse (called "progression-free survival"), as well as how many people's cancer responded to treatment and how long people lived overall. The reported data shows that no numerical results were submitted to ClinicalTrials.gov for any of the outcome measures — including progression-free survival, overall response rate, complete response rate, lymph node response rate, or overall survival. This means that figures for these measurements were not reported in the structured results data available on the registry. Of the participants who started the trial, 53 people in the idelalisib group and 45 people in the placebo group were recorded as having completed it, with the remaining participants noted as not completing the trial; however, no outcome measurement numbers accompanied these figures. Because no outcome data was submitted for either group across any of the planned measures, it is not possible to describe what the trial found in terms of numbers. The reported data shows only that the trial took place and recorded participation figures, but the specific results were not available in the registry entry. These are the results as reported to ClinicalTrials.gov. They are not medical advice — always discuss what they mean for you with your doctor.

These are the results as reported to ClinicalTrials.gov, not medical advice. Verify independently with the trial site and discuss what they mean for you with your doctor.

Phase 3 Lymphoma Trial, Terminated

NCT01732926
Terminated Phase 3 🇦🇺 Australian site

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:

  • You have been diagnosed with a type of slow-growing B-cell lymphoma (a blood cancer), confirmed by a tissue sample test.
  • Your specific type of lymphoma must be one of the following: Follicular Lymphoma (Grade 1, 2, or 3a), Small Lymphocytic Lymphoma (SLL), Lymphoplasmacytoid Lymphoma or Waldenström Macroglobulinemia, or Marginal Zone Lymphoma (in the spleen, lymph nodes, or other areas).

Who may not be able to join:

  • You have a history of a different type of lymphoma or blood cancer not listed in the eligible types above.
  • You currently have or have had certain liver or bile-related conditions, including drug-related liver damage, active hepatitis B or C, alcoholic liver disease, liver scarring (cirrhosis), high blood pressure in the liver, or related conditions (confirm with trial site).
  • You were previously treated with a drug called bendamustine and it did not work for you.

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 13 July 2026
Phase 3: approximately ~65% 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: Gilead Study Director, Gilead Sciences

Australian sites

Prince of Wales Hospital, Randwick, New South Wales
Haematology and Oncology Clinics of Australia Gold Coast, South Brisbane, Queensland
Royal Adelaide Hospital, Adelaide, South Australia
Adelaide Cancer Centre, Kurralta Park, South Australia
Box Hill Hospital, Box Hill, Victoria
Monash Medical Centre, Clayton, Victoria
Saint Vincent's Hospital, Fitzroy, Victoria
Western Hospital, Footscray, Victoria
Royal Perth Hospital, Perth, Western Australia

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

GP referral letter

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Trial details

Status
Terminated
Phase
Phase 3
Sponsor
Registry
ClinicalTrials.gov
Start date
2 January 2013
Est. completion
17 May 2016

Where this trial is recruiting

🇦🇺 Australia 🇨🇦 Canada 🇨🇿 Czechia 🇫🇷 France 🇩🇪 Germany 🇮🇱 Israel 🇮🇹 Italy 🇵🇱 Poland 🇷🇺 Russia 🇰🇷 South Korea 🇪🇸 Spain 🇸🇪 Sweden 🇹🇼 Taiwan 🇬🇧 United Kingdom 🇺🇸 United States

9 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Progression-free Survival (PFS)

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: 13 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