Wednesday, July 8, 2026

Drug profile · INN

icotrokinra hydrochloride

icotrokinra hydrochloride (ICOTYDE) is an FDA-listed pharmaceutical active ingredient. Route of administration: oral. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 2
Pipeline programs 2
News articles 0
Drug details — icotrokinra hydrochloride
US status
approved
Class
Route
ORAL
Patents
2
Programs
2
Data quality
0.84

Quick answer

icotrokinra hydrochloride (ICOTYDE) is an FDA-listed pharmaceutical active ingredient. Route of administration: oral. Current US regulatory status: approved.

Key facts

INN icotrokinra hydrochloride
Brand ICOTYDE
Route ORAL
Formulation TABLET

Approval history

Authority Status Date
FDA approved

Pipeline programs

  1. Icotrokinra Phase 3 · Janssen Cilag International · Crohn Disease
  2. Icotrokinra, JNJ-77242113-AAC Placebo tablet Phase 3 · Janssen-Cilag International N.V · Moderately to Severely Active Ulcerative Colitis

Related patents

  1. US 11939361

    Compositions of peptide inhibitors of Interleukin-23 receptor

    Expires Mon Mar 21 2044 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted
  2. US 11845808

    Peptide inhibitors of interleukin-23 receptor and their use to treat inflammatory diseases

    Expires Mon Dec 14 2043 00:00:00 GMT+0000 (Coordinated Universal Time)

    granted

Frequently asked questions

What is icotrokinra hydrochloride?

icotrokinra hydrochloride (ICOTYDE) is an FDA-listed pharmaceutical active ingredient. Route of administration: oral. Current US regulatory status: approved.

What is the brand name for icotrokinra hydrochloride?

ICOTYDE is a marketed brand name for icotrokinra hydrochloride. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of icotrokinra hydrochloride?

icotrokinra hydrochloride has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.