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Anktiva

Phase 2

Long COVID | Small molecule | Infectious Disease |ImmunityBio, Inc.|Last Updated: May 13, 2026

Success Probability
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Market & Valuation
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Trial Design
UNCONTROLLEDDMC
Total Trials1
Total Enrollment40
FDA Designations
BREAKTHROUGH_THERAPY
Clinical trial landscape

Anktiva · 1 trial · 3 indications

Phase 2 1
NCT07123727A Study to Examine Anktiva for the Treatment of COVID-19.Long COVID
RECRUITING40 Analytics
PHASE2RECRUITING
A Study to Examine Anktiva for the Treatment of COVID-19.
Long COVID
NCT0712372740
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Study Endpoints
Primary Endpoints
Incidence of treatment emergent adverse events (TEAEs) through 30 days post final study drug administration.
Through 30 days post final study drug administration.
Incidence of grade 3 or higher TEAEs through 30 days post final study drug administration.
Through 30 days post final study drug administration.
Incidence of serious adverse events (SAEs) through 30 days post final study drug administration.
Through 30 days post final study drug administration.
Incidence of abnormal changes in safety laboratory tests (CBC and CMP).
Through the end of the study treatment period (approximately 75 days).
Clinically important changes in vital signs such as temperature in degrees Fahrenheit.
Through the end of the study treatment period (approximately 75 days).
Clinically important changes in vital signs such as heart rate in beats per minute.
Through the end of the study treatment period (approximately 75 days).
Clinically important changes in vital signs such as blood pressure in millimeters of mercury (mmHg).
Through the end of the study treatment period (approximately 75 days).
Clinically important changes in vital signs such as respiratory rate in breaths per minute.
Through the end of the study treatment period (approximately 75 days).
Clinically important changes in vital signs such as oxygen saturation in percentage.
Through the end of the study treatment period (approximately 75 days).
Secondary Endpoints
Percent increase or decrease change in the Absolute lymphocyte count (as measured on CBC) from Screening to End Of Study with various timepoints.
Through the end of the study treatment period (approximately 75 days).
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Study Design & Arms
AllocationNA
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT
Treatment Arms
ArmTypeDescription
N-803EXPERIMENTAL -
Interventions
NameTypeDescription
AnktivaDRUG600ug of NAI administered subcutaneously
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Eligibility Criteria
Age Range18 Years to 70 Years
SexALL
Healthy VolunteersNo
Study Sites1

Inclusion Criteria: * Age ≥ 18 and \< 70 years. * History of at least one SARS-CoV-2 infection, defined as report of a positive nucleic acid amplification test (NAAT) and/or a positive SARS-CoV-2 antigen rapid diagnostic test (RDT). Those with only suspected but unconfirmed infections are not eligi...

Countries:United States
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Competitive Landscape -COVID-19 37 trials (matched to "Long COVID")
CompanyTickerTrialsLead PhaseDrugs
Pfizer Inc.PFE8PHASE3ibuzatrelvir, remdesivir
BioNTech SE Sponsored ADRBNTX3PHASE3BNT162b2
Merck & Co., Inc.MRK1PHASE3Molnupiravir
Invivyd, Inc.IVVD2PHASE3VYD2311-SD, VYD2311-MD
Vanda Pharmaceuticals Inc.VNDA1PHASE3Tradipitant
BioVie Inc. Class ABIVI1PHASE2NE3107
ImmunityBio IncIBRX2PHASE2Anktiva
Traws Pharma, Inc.TRAW1PHASE2Ratutrelvir non-randomised, Paxlovid, Ratutrelvir
GeoVax Labs, Inc.GOVX1PHASE2COVID-19 Vaccine, Synthetic MVA-based SARS-CoV-2 Vaccine GEO-CM04S1
Unity Health TorontoUBX1PHASE3Paxlovid, Antioxidant
Moderna, Inc.MRNA1 - SPIKEVAX Bivalent BA.1, SPIKEVAX XBB.1.5, SPIKEVAX JN.1
Abbott LaboratoriesABT1N/AUndisclosed
Design Therapeutics, Inc.DSGN1EARLY_PHASE1COVID-19 Therapeutic Biologic Mix - NOVAVAX COVID-19 VACCINE plus BCG Vaccine Mix for percutaneous use
Jade Biosciences, Inc.JBIO1N/AUndisclosed
Structure Therapeutics, Inc. Sponsored ADRGPCR1N/AUndisclosed
Co-Diagnostics, Inc.CODX1 - Undisclosed
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Recent Changes (Last 90 Days)
LOWMay 26, 2026NCT07123727primaryCompletionDate: changed
LOWMay 24, 2026NCT07123727studyFirstPostDate: changed