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Rhizen Pharmaceuticals
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Country
Switzerland
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Address
Fritz-Courvoisier 40, CH-2300 La Chaux-de-Fonds
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Telephone
+41 32 580 0113
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Tenalisib (RP6530, selective dual PI3K d/γ inhibitor with additional SIK3 inhibitory activity) showed encouraging results with a clinical benefit rate (CBR) of 57.5% from an ongoing phase II trial in patients with locally advanced or metastatic HR+/HER2- breast cancer (mBC).


Lead Product(s): Tenalisib

Therapeutic Area: Oncology Product Name: RP6530

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 09, 2022

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Rhizen indicated that RP12146 has comparable preclinical activity vis-à-vis approved PARP inhibitors and shows improved preclinical safety that it expects will translate in the clinic.


Lead Product(s): RP12146

Therapeutic Area: Oncology Product Name: RP12146

Highest Development Status: Phase I/ Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 01, 2021

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RP7214, a small molecule oral dihydroorotate dehydrogenase (DHODH) inhibitor with reduced nanomolar potency, in Covid-19 patients with mild, symptomatic disease.


Lead Product(s): RP7214

Therapeutic Area: Infections and Infectious Diseases Product Name: RP7214

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 21, 2021

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Umbralisib (UKONIQ) granted accelerated approval by US FDA for the treatment of adult patients with relapsed or refractory marginal zone lymphoma (MZL), follicular lymphoma (FL).


Lead Product(s): Umbralisib

Therapeutic Area: Oncology Product Name: Ukoniq

Highest Development Status: ApprovedProduct Type: Small molecule

Recipient: TG Therapeutics

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 08, 2021

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UKONIQ is the first and only, oral, once daily, inhibitor of phosphoinositide 3 kinase delta and casein kinase 1 epsilon. UKONIQ is approved for adult patients with relapsed or refractory marginal zone lymphoma after at least one prior anti-CD20 based regimen.


Lead Product(s): Umbralisib

Therapeutic Area: Oncology Product Name: Ukoniq

Highest Development Status: ApprovedProduct Type: Small molecule

Recipient: TG Therapeutics

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 05, 2021

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Tenalisib (RP6530) is a highly selective and orally active dual PI3K delta/gamma inhibitor with efficient translation of activity through enzyme, cell, and whole blood-based studies.


Lead Product(s): Tenalisib

Therapeutic Area: Oncology Product Name: RP6530

Highest Development Status: Phase I/ Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 22, 2021

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Curon obtains the exclusive development and commercialization rights of Tenalisib for Greater China across all oncology indications, and will lead the clinical development in that territory.


Lead Product(s): Tenalisib

Therapeutic Area: Oncology Product Name: RP6530

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Curon Biopharmaceutical

Deal Size: $149.5 million Upfront Cash: Undisclosed

Deal Type: Licensing Agreement October 12, 2020

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Single-agent Tenalisib was well tolerated with a good overall response rate (ORR) in both peripheral and cutaneous T-cell Lymphoma patients (PTCL and CTCL).


Lead Product(s): Tenalisib

Therapeutic Area: Oncology Product Name: RP6530

Highest Development Status: Phase I/ Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 24, 2020

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