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Epizyme
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400 Technology Square, 4th Floor Cambridge, MA 02139
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(617) 229-5872

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Ipsen acquires Epizyme’s lead medicine, Tazverik® (tazemetostat), a first-inclass, chemotherapy-free EZH2a inhibitor, which was granted Accelerated Approval by the U.S. Food and Drug Administration (FDA) in 2020.


Lead Product(s): Tazemetostat

Therapeutic Area: Oncology Product Name: Tazverik

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Ipsen

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Acquisition August 12, 2022

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The primary focus of the acquisition is on the lead medicine, Tazverik® (tazemetostat), a first-in-class, chemotherapy-free EZH2[1] inhibitor, which was granted Accelerated Approval by the U.S. Food and Drug Administration (FDA) in 2020.


Lead Product(s): Tazemetostat

Therapeutic Area: Oncology Product Name: Tazverik

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Ipsen

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Acquisition June 27, 2022

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Treatment with Tazverik (tazemetostat) and R2 was generally well tolerated and the adverse events were consistent with those contained in the prescribing information for both tazemetostat and R2, respectively.


Lead Product(s): Tazemetostat,Rituximab,Lenalidomide

Therapeutic Area: Oncology Product Name: Tazverik

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 02, 2022

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TAZVERIK (tazemetostat), is a methyltransferase inhibitor of EZH21 is approved by the FDA for the treatment of certain patients with ES and certain patients with FL.


Lead Product(s): Tazemetostat

Therapeutic Area: Oncology Product Name: Tazverik

Highest Development Status: ApprovedProduct Type: Small molecule

Recipient: Hutchmed

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 01, 2022

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TST001 is a high affinity humanized anti-Claudin18.2 monoclonal antibody with enhanced antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC) activities and potent anti-tumor activities in tumor xenograft models.


Lead Product(s): TST001,Capecitabine,Oxaliplatin

Therapeutic Area: Oncology Product Name: TST001

Highest Development Status: Phase IProduct Type: Large molecule

Recipient: Transcenta Holding

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 01, 2022

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First patient dosed in the randomized portion of symphony-1 (EZH-302), epizyme’s phase 1B/3 confirmatory study of Tazverik (tazemetostat) in combination with rituximab + lenalidomide (R2) for the treatment of follicular lymphoma.


Lead Product(s): Tazemetostat,Lenalidomide,Rituximab

Therapeutic Area: Oncology Product Name: Tazverik

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 15, 2022

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Epizyme anticipates using the net proceeds from the offering, together with its existing cash, cash equivalents and marketable securities, to fund global development and commercialization costs of tazemetostat outside of Japan.


Lead Product(s): Tazemetostat,Doxorubicin Hydrochloride

Therapeutic Area: Oncology Product Name: Tazverik

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Jefferies

Deal Size: $85.0 million Upfront Cash: Undisclosed

Deal Type: Public Offering January 27, 2022

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Among the 13 patients evaluated in this standard dose escalation design, no Dose Limiting Toxicities (DLTs) were observed during the first cycle of treatment up to the highest dose of 800mg of TAZVERIK twice daily.


Lead Product(s): Tazemetostat

Therapeutic Area: Oncology Product Name: Tazverik

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 02, 2021

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Details:

The expanded loan facility is a part of the original loan agreement where Epizyme drew down $70 million to fund the regulatory milestones owed to Eisai for the New Drug Application submissions and U.S. FDA approvals of TAZVERIK® for epithelioid sarcoma and follicular lymphoma.


Lead Product(s): Tazemetostat

Therapeutic Area: Oncology Product Name: Tazverik

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Pharmakon Advisors

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Financing November 06, 2020

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Data supported the accelerated approval of TAZVERIK by the U.S. FDA for the treatment of epithelioid sarcoma in January 2020, and the accelerated approval of TAZVERIK by the FDA for the treatment of relapsed/refractory follicular lymphoma in June 2020.


Lead Product(s): Tazemetostat

Therapeutic Area: Oncology Product Name: Tazverik

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 07, 2020

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