Dashboard PDUFA PDUFA History Dilution Watch Downside Radar Missed Milestones Earnings Big Movers Blog

🎤 Upcoming Biotech Conferences

Loading conferences...
Free to browse, no account needed Follow the companies behind these drugs with free AI briefings, catalyst countdowns and dilution alerts.

RI-002 · Asceniv

Plasma-derived product · Immune activation · developed by ADMA Biologics

Approved FDA, Apr 2019
ADMA Developer
1 Registered trials

What is RI-002?

Asceniv is an intravenous immune globulin derived from human plasma. It provides passive immunotherapy by supplying immunoglobulins to patients with primary immune deficiency disorders.

Summary written with AI from the sources listed at the end of this page.

At a glance

Also known as
Asceniv, Immune Globulin (Human)
Drug type
Plasma-derived product
Mechanism
Immune activation
Therapy area
Immunology
Developer
ADMA Biologics, Inc. (ADMA)
FDA status
Approved as Asceniv (April 1, 2019), BLA125590
UNII
78I1W13C3D

🧪 Clinical trials

TrialPhaseConditionStatusSponsor
NCT01814800 Phase 3 Primary Immune Deficiency Disorder Completed ADMA

Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.

Conditions studied

Primary Immune Deficiency Disorder

More from ADMA Biologics

Sources

Updated Oct 3, 2026. Something wrong or missing? Report it on the ADMA page.

Follow ADMA, the company behind RI-002

See ADMA's upcoming FDA decisions, trial readouts, cash runway and dilution risk, updated every day from SEC, FDA and ClinicalTrials.gov filings.

ADMA catalysts and pipeline →
Data: FDA (Drugs@FDA, Purple Book, DailyMed), NIH (NCI Thesaurus, GSRS, RxNorm), ClinicalTrials.gov • Informational purposes only, not medical or investment advice. • All drugs A–Z

This data is for informational purposes only, not investment advice. BioRadar does not provide buy/sell recommendations. Past performance does not guarantee future results. Always do your own due diligence.