Clinical Trials Information
As a biopharmaceutical company, Nektar Therapeutics conducts preclinical and clinical studies of our investigational medicines to evaluate them for both safety and efficacy. We focus our efforts on medical conditions where currently approved medicines are not providing optimal therapeutic benefit.
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 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, and play a vital role in advancing medicine.
Nektar Therapeutics is currently recruiting patients in the U.S. and other countries for the following clinical trials. Please follow the links below for more information on the enrollment criteria for each study and site location:
A Phase 3, Randomized, Study of Neoadjuvant and Adjuvant Nivolumab Plus NKTR-214, Versus Nivolumab Alone Versus Standard of Care in Participants With Muscle-Invasive Bladder Cancer (MIBC) Who Are Cisplatin Ineligible
A Dose Escalation and Cohort Expansion Study of CD122-Biased Cytokine (NKTR-214) in Combination With Anti-PD-1 Antibody (Nivolumab) or in Combination With Nivolumab and Anti-CTLA4 Antibody (Ipilimumab) in Patients With Select Advanced or Metastatic Solid Tumors (PIVOT-02)
JAVELIN IL-2 Medley
A Phase 1b/2 Study to Evaluate Safety and Clinical Activity of Avelumab in Combination With Bempegaldesleukin (NKTR-214) With or Without Talazoparib or Enzalutamide in Participants With Locally Advanced or Metastatic Solid Tumors
ONZEALD® (etirinotecan pegol)
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).