Clinical Trials Information
Nektar Therapeutics is focused on the clinical development of our investigational medicines to evaluate them for both safety and efficacy, especially for medical conditions where there are no effective approved medicines.
Before a new therapy can be made available to the general public, rigorous tests involving multiple studies on human volunteers are required. These studies, referred to as clinical trials, are carefully conducted and are regulated by the Food and Drug Administration (FDA) in the United States and by similar regulatory agencies worldwide. Participation in clinical trials allows patients to potentially gain access to the latest investigational treatments at little to no cost, while also playing a vital role in advancing medicine.
Nektar Therapeutics is recruiting patients in the U.S. and other countries for the following active clinical trials. Please follow the links below for more information on the enrollment criteria for each study and site location:
Rezpegaldesleukin (REZPEG/NKTR-358)
More information on REZPEG (NKTR-358)
NKTR-255
Bempegaldesleukin (BEMPEG/NKTR-214)
In April 2022, Nektar Therapeutics and Bristol Myers Squibb announced that the companies have jointly decided to end the global clinical development program for bempegaldesleukin in combination with Opdivo. These studies and all other ongoing studies in the program will be discontinued, allowing patients and their physicians to consider standard of care treatment options for their specific conditions.
More information on Bempegaldesleukin
Further information and background on clinical trials may be found on www.clinicaltrials.gov, a service of the U.S. National Institutes of Health (NIH).
