Phase 3 Pancreatic Cancer Trial, Completed NCT01231347 Sponsor: NantCell, Inc. Condition: Pancreatic Cancer
Back to Pancreatic Cancer

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 involved 800 people with advanced (metastatic) pancreatic cancer. Participants were divided into three groups: one group received a placebo (an inactive substance) plus the chemotherapy drug gemcitabine (322 people), a second group received a medicine called AMG 479 at a lower dose (12 mg/kg) plus gemcitabine (318 people), and a third group received AMG 479 at a higher dose (20 mg/kg) plus gemcitabine (160 people). The trial was measuring overall survival — that is, how long participants lived from the time they joined the study. The reported data shows that the median overall survival — meaning the point at which half of the participants in each group had passed away and half were still alive — was very similar across all three groups. The lower-dose AMG 479 group had a median survival of 7.0 months, the higher-dose AMG 479 group had 7.1 months, and the placebo group had 7.2 months. No secondary outcome measure data was included in the results submitted to ClinicalTrials.gov, so those figures cannot be reported here. It is also worth noting that a large proportion of participants did not complete the study in each group — this is not unusual in trials involving people with advanced cancer, but the reasons were not detailed in the submitted data. 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 Pancreatic Cancer Trial, Completed

NCT01231347
Completed 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 pancreatic cancer (specifically adenocarcinoma) that has spread to other parts of the body and has not yet been treated.
  • Your blood counts, kidneys, and liver are working well enough to meet the trial's health requirements.
  • You are generally able to carry out normal daily activities with little or no limitation (confirm with trial site).

Who may not be able to join:

  • You have already received chemotherapy or radiation therapy for your pancreatic cancer.
  • Your cancer has spread to the brain or spinal cord area.
  • You currently have an external drain for bile (a tube placed outside the body to drain bile).

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 2 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.

GP referral letter

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

Trial details

Status
Completed
Phase
Phase 3
Sponsor
NantCell, Inc.
Registry
ClinicalTrials.gov
Start date
7 April 2011
Est. completion
12 December 2012

Where this trial is recruiting

🇦🇺 Australia 🇦🇹 Austria 🇧🇪 Belgium 🇧🇷 Brazil 🇧🇬 Bulgaria 🇨🇦 Canada 🇨🇿 Czechia 🇩🇰 Denmark 🇫🇮 Finland 🇫🇷 France 🇩🇪 Germany 🇬🇷 Greece Hong Kong 🇭🇺 Hungary 🇮🇹 Italy 🇯🇵 Japan 🇱🇹 Lithuania 🇳🇱 Netherlands 🇵🇱 Poland 🇵🇹 Portugal 🇷🇴 Romania 🇷🇺 Russia 🇷🇸 Serbia 🇸🇰 Slovakia 🇸🇮 Slovenia 🇰🇷 South Korea 🇪🇸 Spain 🇸🇪 Sweden 🇨🇭 Switzerland 🇹🇼 Taiwan 🇬🇧 United Kingdom 🇺🇸 United States

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

Primary endpoints

Determine if the Treatment of AMG 479 at 12 mg/kg and/or 20 mg/kg in Combination With Gemcitabine Improves Overall Survival as Compared With Placebo in Combination With Gemcitabine in Subjects With Metastatic Adenocarcinoma of the Pancreas

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: 2 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