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Immunitybio Inc (IBRX)
NASDAQ:IBRX
US Market
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ImmunityBio (IBRX) Drug Pipeline

2,500 Followers
Drug Name
Condition
Stage
Status
Study Name
Trial Start Date
Article
Cisplatin, Nab-Paclitaxel, Nogapendekin Alfa Inbakicept, Had5-Hpv Vaccine, De-Intensified Imrt, Standard Of Care Imrt
Head And Neck Cancer, Oropharyngeal Squamous Cell Carcinoma, Hpv-Positive Oropharyngeal Squamous Cell Carcinoma
Phase II
Not Yet Recruiting
Phase 2 Study of NAI, HPV Vaccine, and Nab-Paclitaxel in HPV-Positive Oropharyngeal Cancer Followed by De-Intensified Radiation Compared With Standard Chemoradiation
Jun 01, 2026
Bcg, Bcg Plus Anktiva
Nmibc
Phase III
Withdrawn
ANKTIVA Plus BCG Versus BCG Monotherapy In Participants With BCG-Naïve/BCG-Exposed High-Grade Non-Muscle Invasive Papillary Bladder Cancer
Apr 20, 2026
Nogapendekin Alfa-Inbakicept, Allogeneic Invariant Natural Killer T Cells, N-803, Alt-803, Anktiva
Severe Community-Acquired Pneum, Lymphopenia / Immunoparalysis In Critically Ill Adults, Acute Respiratory Distress Syndrome, Sepsis
Phase II
Withdrawn
Nogapendekin Alfa-Inbakicept and iNKT Cells for Critically Ill Adults With Severe Community-Acquired Pneumonia (With or Without Sepsis/ARDS)
Mar 13, 2026
N-803, Anktiva, Nogapendekin Alfa Inbakicept, Sotevtamab, Zabadinostat, Nab Paclitaxel / Gemcitabine
Pancreatic Cancer, Pancreatic Cancer Resectable
Phase I
Not Yet Recruiting
Open-Label, Phase 1 Clinical Trial of Neoadjuvant Nogapendekin Alfa Inbakicept, Sotevtamab, and Zabadinostat in Combination With Gemcitabine and Nab-Paclitaxel for Participants With Borderline Resectable or Locally Advanced Pancreatic Cancer
Nov 20, 2025
Nogapendekin Alfa Inbakicept, Agent-797
Immunoparalysis, Lymphopenia, Acute Respiratory Distress Syndrome (Ards), Sepsis, Community-Acquired Pneumonia (Cap)
Phase III
Withdrawn
Study of Nogapendekin Alfa Inbakicept and iNKT Cells in Critically Ill Adults With Severe Community-Acquired Pneumonia
Sep 18, 2025
Cd19 T-Hank- Iv Administration
Relapsed B-Cell Non Hodgkin Lymphoma
Phase II
Not Yet Recruiting
Open Label, Phase 2 Study of CD19t-haNK and N-803 in Combination With Rituximab in Participants With Relapsed/ Refractory B-cell Non- Hodgkin Lymphoma.
Aug 11, 2025
N-803
Long Covid
Phase II
Recruiting
A Study to Assess Anktiva in Patients With Long Covid-19.
Jul 30, 2025
Anktiva
Long Covid, Long Covid Syndrome, Long Covid 19
Phase II
Recruiting
A Study to Examine Anktiva for the Treatment of COVID-19.
Jul 30, 2025
N-803 And Bcg, N-803 And Gemcitabine
Non-Muscle Invasive Bladder Cancer (Nmibc)
Phase II
Not Yet Recruiting
Clinical Trial of Ablation Therapy in Participants With Intermediate-Risk Non-Muscle Invasive Papillary Bladder Cancer
Feb 05, 2025
Intravesical Recombinant Mycobacterium
Nmibc
Phase I/II
Recruiting
ResQ133A-NMIBC: Intravesical Recombinant Mycobacterium (rMBCG) in Participants With NMIBC Eligible to Receive Intravesical Tice BCG
Jan 24, 2025

FAQ

What are the FDA phases for drug approval?
The FDA approval process for new drugs is divided into several phases:
a. Preclinical testing
b. Phase 1 – Safety and dosage
c. Phase 2 – Effectiveness and side effects
d. Phase 3 – Confirmation of effectiveness, monitoring of adverse reactions, and comparison with existing treatments
e. Phase 4 – Post-marketing studies to track long-term safety and effectiveness
    What is a clinical trial?
    A clinical trial is a carefully designed study in which researchers test a drug, treatment, or medical device in people to evaluate its safety, effectiveness, and potential side effects. These trials are essential for determining whether a new treatment should be approved for widespread use.
      What drugs does Immunitybio Inc (IBRX) have in its pipeline
      IBRX is currently developing the following drugs: Cisplatin, Nab-Paclitaxel, Nogapendekin Alfa Inbakicept, Had5-Hpv Vaccine, De-Intensified Imrt, Standard Of Care Imrt, Bcg, Bcg Plus Anktiva, Nogapendekin Alfa-Inbakicept, Allogeneic Invariant Natural Killer T Cells, N-803, Alt-803, Anktiva. These drug candidates are in various stages of clinical development as the company works toward FDA approval.