TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

SCEMBLIX

ASCIMINIB HYDROCHLORIDE
Oncology Approved 2021-10-29
6
Indications
--
Phase 3 Trials
3
Priority Reviews
4
Years on Market

Details

Status
Prescription
First Approved
2021-10-29
Routes
ORAL
Dosage Forms
TABLET

Companies

Active Ingredient: ASCIMINIB HYDROCHLORIDE

SCEMBLIX Approval History

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What SCEMBLIX Treats

1 indications

SCEMBLIX is approved for 1 conditions since its original approval in 2021. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Chronic Myeloid Leukemia
Source: FDA Label

SCEMBLIX Competitors

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2 other drugs also target ABL. Compare mechanisms, indications, and trial activity.

Drug = Competitor name Company = Manufacturer N indic. = FDA-approved indications โ†’ Date = Patent/exclusivity expiry

Competitors share the same molecular target (ABL). Earlier expiry dates signal biosimilar/generic opportunities.

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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.

SCEMBLIX FDA Label Details

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Indications & Usage

FDA Label (PDF)

SCEMBLIX is indicated for the treatment of adult patients with: Newly diagnosed Philadelphia chromosome-positive chronic myeloid leukemia (Ph+ CML) in chronic phase (CP). This indication is approved under accelerated approval based on major molecular response rate [see Clinical Studies ] . Continued approval for this indication may be contingent upon verification of clinical benefit in a confirmatory trial(s). Previously treated Ph+ CML in CP. Ph+ CML in CP with the T315I mutation. SCEMBLIX is a kinase inhibitor indicated for the treatment of adult patients with: Newly diagnosed Philadelphia c...

SCEMBLIX Patents & Exclusivity

Latest Patent: May 2040
Exclusivity: Oct 2031

Patents (36 active)

US12252479 Expires May 17, 2040
US12252478 Expires May 14, 2040
US11407735 Expires May 14, 2040
US8829195 Expires Oct 29, 2035
+ 26 more patents

Exclusivity

I-953 Until Oct 2027
I-954 Until Oct 2027
M-318 Until Oct 2028
NCE Until Oct 2026
ODE-381 Until Oct 2028
Source: FDA Orange Book

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Data Sources

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