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Priya Life Science Compound trial record
Compound · clinical trials

Anktiva clinical trials

Also listed in trial records as N-803, Nogapendekin Alfa Inbakicept, N803, ALT-803, IL-15 Superagonist
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 14 trials in our USA, Mexico, UK, Canada, India and Egypt registers that name Anktiva as an intervention. Synced 9 Nov 2026
14Current trials
5Recruiting now
2Lead sponsors
6Country registers
At a glance

Anktiva is named as an intervention in 14 current clinical trials in our USA, Mexico, UK, Canada, India and Egypt registers. 5 are recruiting patients now. The most common phase is Phase 2. The sponsor with the most trials is ImmunityBio, Inc (13). The most-studied condition is Urothelial Carcinoma.

Where Anktiva is approved

All regulators →

Of the three regulators tracked here, the first to approve Anktiva was the US, on 22 Apr 2024. It is approved in 2 of the 3 regulators tracked here.

USUnited States (FDA)
22 Apr 2024
Anktiva
BLA761336 on Drugs@FDA
First original NDA/BLA approval
EUEuropean Union (EMA)
16 Feb 2026
Anktiva
EMA product page
First centralised authorisation
CACanada (Health Canada)
No new-drug Notice of Compliance since 1994
First new-drug NOC

From the regulators' own registers: FDA Drugs@FDA, the EMA medicines list and Health Canada's Notice of Compliance database. Dates are the first listed approval of a product containing only this substance; combination products and nationally authorised EU medicines are not counted.

NICE appraisals of Anktiva

All NICE appraisals →

NICE, which decides whether the NHS in England should fund new medicines, has published 1 technology appraisal of Anktiva. 1 is current.

AppraisalNICE recommendationPublishedStatus
Nogapendekin alfa inbakicept with BCG for non-muscle-invasive bladder cancer with carcinoma in situ that is unresponsive to BCG (terminated evaluation)
NICE TA1163
Terminated (no company submission)4 Jun 2026Current

NICE decisions apply to the NHS in England. In Ireland the HSE decides on reimbursement, advised by the National Centre for Pharmacoeconomics. Titles, categories and dates link to the guidance on nice.org.uk. © NICE 2026 technology appraisal guidance. Available from www.nice.org.uk/guidance. All rights reserved. Subject to Notice of rights. NICE guidance is prepared for the National Health Service in England. All NICE guidance is subject to regular review and may be updated or withdrawn. NICE accepts no responsibility for the use of its content in this product/publication.

Patient leaflets for Anktiva

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • EU
    European Union: Anktiva
    EMA product information: package leaflet and summary of product characteristics in every EU language.
  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Trials by status

  • Recruiting536%
  • Not yet open17%
  • Active, closed857%

Trials by phase

  • Phase 2643%
  • Phase 1321%
  • Phase 2/3214%
  • Phase 317%
  • Phase 1/217%
  • Observational17%
01

Clinical trials of Anktiva

14 trials
StudyPhaseStatusLead sponsorRegisters
Clinical Trial of N-803 Plus Tislelizumab or Prior Failed Immune Checkpoint Inhibitor and Docetaxel Versus Docetaxel Monotherapy in Participants With Advanced or Metastatic Non-Small Cell Lung Cancer Who Have Acquired Resistance to Immune Checkpoint Inhibitor Therapy
NCT06745908 · NSCLC Stage IV
Phase 3 Recruiting ImmunityBio, Inc UK, USA, Canada
A Phase 2, Open-label, Single-arm Study Of Autologous M-CENK Adoptive Cell Therapy And N-803 (IL-15 Superagonist) In Combination With Gemcitabine In Participants With Recurrent Platinum-Resistant High-Grade Ovarian Cancer
NCT06710288 · Platinum-resistant Ovarian Cancer
Phase 2 Recruiting ImmunityBio, Inc USA
A Study to Assess Anktiva in Patients With Long Covid-19.
NCT07108036 · Long COVID
Phase 2 Recruiting ImmunityBio, Inc USA
A Study to Examine Anktiva for the Treatment of COVID-19.
NCT07123727 · Long COVID, Long COVID Syndrome, Long Covid 19
Phase 2 Recruiting ImmunityBio, Inc USA
Study for Subjects With Relapsed/Refractory Non- Hodgkin Lymphoma
NCT05618925 · Non Hodgkin's Lymphoma Refractory/Relapsed
Phase 1 Recruiting ImmunityBio, Inc USA
N-803 in Combination With Pembrolizumab and Enfortumab Vedotin for Treatment of Urothelial Cancer
NCT07217496 · Metastatic Urothelial Carcinoma, Urothelial Carcinoma, Locally Advanced Urothelial Carcinoma
Phase 1 Not yet open ImmunityBio, Inc USA
QUILT-3.032: A Multicenter Clinical Trial of Intravesical Bacillus Calmette-Guerin (BCG) in Combination With ALT-803 (N-803) in Patients With BCG Unresponsive High Grade Non-Muscle Invasive Bladder Cancer
NCT03022825 · Bladder Cancer
Phase 2/3 Active, closed ImmunityBio, Inc USA
Testing the Use of Combination Immunotherapy Treatment (N-803 [ALT-803] Plus Pembrolizumab) Against the Usual Treatment for Advanced Non-small Cell Lung Cancer (A Lung-MAP Treatment Trial)
NCT05096663 · ClinicalTrials.gov ↗ · Advanced Lung Non-Small Cell Carcinoma, Recurrent Lung Non-Small Cell Carcinoma, Stage III Lung Cancer AJCC v8
Phase 2/3 Active, closed SWOG Cancer Research Network Mexico, Egypt
QUILT-3.055: A Study of Combination Immunotherapies in Patients Who Have Previously Received Treatment With Immune Checkpoint Inhibitors
NCT03228667 · Non-Small Cell Lung Cancer, Small Cell Lung Cancer, Urothelial Carcinoma
Phase 2 Active, closed ImmunityBio, Inc USA
Combination Immunotherapy Plus Standard-of-Care Chemotherapy Versus Standard-of-Care Chemotherapy for the Treatment of Locally Advanced or Metastatic Pancreatic Cancer
NCT04390399 · Pancreatic Cancer
Phase 2 Active, closed ImmunityBio, Inc USA
N-803 and PD-L1 t-haNK Combined With Bevacizumab for Recurrent or Progressive Glioblastoma
NCT06061809 · Glioblastoma
Phase 2 Active, closed ImmunityBio, Inc USA
A Study of Intravesical BCG in Combination With ALT-803 in Patients With Non-Muscle Invasive Bladder Cancer
NCT02138734 · Non-muscle Invasive Bladder Cancer
Phase 1/2 Active, closed ImmunityBio, Inc USA, India, Mexico
QUILT-3.076: Study of Autologous M-CENK in Subjects With Locally Advanced or Metastatic Solid Tumors
NCT04898543 · Metastatic Solid Tumor
Phase 1 Active, closed ImmunityBio, Inc USA
Follow up of Intravesical N-803 Plus BCG in BCG-Naive Non-Muscle Invasive Bladder Cancer (NMIBC)
NCT05981131 · Non Muscle Invasive Bladder Cancer
Observational Active, closed ImmunityBio, Inc USA

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with Anktiva

23 conditions
Urothelial Carcinoma2Long COVID2NSCLC Stage IV1Metastatic Urothelial Carcinoma1Locally Advanced Urothelial Carcinoma1Urothelial Cancer1Long COVID Syndrome1Long Covid 191Metastatic Solid Tumor1Pancreatic Cancer1Platinum-resistant Ovarian Cancer1Non-Small Cell Lung Cancer1
All 23 conditions
Condition (as registered)Trials
Urothelial Carcinoma2
Long COVID2
NSCLC Stage IV1
Metastatic Urothelial Carcinoma1
Locally Advanced Urothelial Carcinoma1
Urothelial Cancer1
Long COVID Syndrome1
Long Covid 191
Metastatic Solid Tumor1
Pancreatic Cancer1
Platinum-resistant Ovarian Cancer1
Non-Small Cell Lung Cancer1
Small Cell Lung Cancer1
Head and Neck Squamous Cell Carcinoma1
Bladder Cancer1
Non-muscle Invasive Bladder Cancer1
Glioblastoma1
Advanced Lung Non-Small Cell Carcinoma1
Recurrent Lung Non-Small Cell Carcinoma1
Stage III Lung Cancer AJCC v81
Stage IIIA Lung Cancer AJCC v81
Non Hodgkin's Lymphoma Refractory/Relapsed1
Non Muscle Invasive Bladder Cancer1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
ImmunityBio, Inc13
SWOG Cancer Research Network1
04

By country register

RegisterTrialsRecruiting
Clinical trials in USA135
Clinical trials in Mexico20
Clinical trials in UK11
Clinical trials in Canada11
Clinical trials in India10
Clinical trials in Egypt10

A trial with sites in more than one country appears in each of those registers.

05

Related compounds

06

Questions about Anktiva trials

How many clinical trials are testing Anktiva?

14 current trials in our USA, Mexico, UK, Canada, India and Egypt registers name Anktiva (also registered as N-803) as a drug or biological intervention, as of the registry sync on 9 November 2026. Completed and withdrawn studies are not counted.

Are Anktiva trials recruiting patients?

Yes. 5 of the 14 trials are recruiting: 5 with sites in USA, 1 with sites in UK and 1 with sites in Canada. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Anktiva clinical trials?

ImmunityBio, Inc (13) and SWOG Cancer Research Network (1). The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Anktiva works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how Anktiva works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Anktiva (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 9 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.