MedPath

Tazemetostat

Generic Name
Tazemetostat
Brand Names
Tazverik
Drug Type
Small Molecule
Chemical Formula
C34H44N4O4
CAS Number
1403254-99-8
Unique Ingredient Identifier
Q40W93WPE1

Overview

Tazemetostat is a methyltransferase inhibitor used to treat metastatic or locally advanced epithelioid sarcoma not eligible for complete resection. Tazemetostat was first named in literature as EPZ-6438. Tazemetaostat was granted FDA approval on 23 January 2020.

Indication

Tazemetostat is indicated to treat adult and pediatric patients 16 years and older with metastatic or locally advanced epithelioid sarcoma that is not eligible for complete resection. It is also indicated to treat adult patients with relapsed or refractory follicular lymphoma whose tumors are positive for an IZH2 mutation and who have received at least 2 prior systemic therapies. Additionally, it is indicated in adult patients with relapsed or refractory follicular lymphoma who have no satisfactory alternative treatment options.

Associated Conditions

  • Locally Advanced Epithelioid Sarcoma
  • Metastatic Epithelioid Sarcoma
  • Refractory Follicular Lymphoma
  • Relapsed Follicular Lymphoma

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2025/02/13
Phase 1
Recruiting
2024/11/18
Phase 2
Recruiting
Eric Jacobsen, MD
2024/08/28
Phase 2
Recruiting
City of Hope Medical Center
2024/02/05
Phase 2
Active, not recruiting
2023/10/05
Phase 2
Not yet recruiting
2023/08/16
Phase 2
Recruiting
2023/08/09
Phase 1
Not yet recruiting
2023/07/07
Phase 1
Recruiting
2023/06/06
Phase 2
Recruiting
2023/02/06
Phase 2
Completed

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Epizyme, Inc.
72607-100
ORAL
200 mg in 1 1
12/21/2023

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.

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