TheraRadar
Data updated: May 26, 2026

REVCOVI (elapegademase-lvlr)

Orphan Drug Priority Review Fast Track
Rare Disease Approved 2018-10-05

REVCOVI is indicated for the treatment of Adenosine Deaminase Severe Combined Immunodeficiency.

Source: FDA Label • CHIESI USA INC

How REVCOVI Works

The medication provides an exogenous source of the ADA enzyme to facilitate the metabolism of adenosine and deoxyadenosine into inosine and deoxyinosine. In patients with ADA deficiency, the accumulation of these compounds leads to the death of thymocytes and a failure in immune cell differentiation. By lowering these toxic nucleotide levels, the drug helps increase lymphocyte counts and supports proper immune system function.

1
Indication
--
Phase 3 Trials
7
Years on Market

Details

Status
Prescription
First Approved
2018-10-05
Patent Cliff
2025

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Patent cliff and revenue data

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Routes
INJECTION
Dosage Forms
INJECTABLE

Companies

Active Ingredient: ELAPEGADEMASE-LVLR

REVCOVI Approval History

2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
2 FDA actions from 2018 to 2020
Dec 2020 SUPPL
Label · Labeling
Oct 2018 ORIGINAL
New Drug · Type 1 - New Molecular Entity

What REVCOVI Treats

1 indications

REVCOVI is approved for 1 conditions since its original approval in 2018. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Adenosine Deaminase Severe Combined Immunodeficiency
Source: FDA Label

REVCOVI Competitive Set

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Three rings of competition based on shared molecular targets and treated indications.

MoA expansion candidates

1

Same target(s), different indications — where else is this mechanism being explored?

Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.

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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

REVCOVI FDA Label Details

Indications & Usage

FDA Label (PDF)

REVCOVI is indicated for the treatment of Adenosine Deaminase Severe Combined Immunodeficiency.

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.