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Napo EU
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Country
Italy
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Address
Corso Giacomo Matteotti Milano (MI), CAP 20121
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Telephone
(415) 963-9938

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Crofelemer is a plant-based drug extracted & purified from the red bark sap. It is being developed for relief and treatment of moderate-to-severe diarrhea, with or without concomitant antimicrobial therapy from bacterial, viral & parasitic infections including Vibrio cholerae.


Lead Product(s): Crofelemer

Therapeutic Area: Gastroenterology Product Name: Undisclosed

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 February 12, 2024

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Mytesi (crofelemer) is a CFTR/CaCC inhibitor small molecule drug administered orally as a delayed release tablet, for prophylaxis of diarrhea in cancer patients.


Lead Product(s): Crofelemer

Therapeutic Area: Gastroenterology Product Name: Mytesi

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 December 11, 2023

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Under the agreement, Napo grants Quadri Pharma exclusive promotional, commercialization, and distribution rights for a powder formulation of Mytesi (crofelemer), the only oral FDA-approved prescription drug under botanical guidance, for oral solution.


Lead Product(s): Crofelemer

Therapeutic Area: Gastroenterology Product Name: Mytesi

Highest Development Status: Phase IProduct Type: Small molecule

Partner/Sponsor/Collaborator: Quadri Pharmaceuticals

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Licensing Agreement November 02, 2023

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Mytesi (crofelemer) powder for oral solution inhibits both cAMP-stimulated CFTR chloride ion channel and the CaCC at the luminal membrane of enterocytes, which being investigated for the treatment of microvillus inclusion disease.


Lead Product(s): Crofelemer

Therapeutic Area: Genetic Disease Product Name: Mytesi

Highest Development Status: IND EnablingProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable August 09, 2023

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Mytesi, only oral plant-based prescription medicine approved under FDA Botanical Guidance, is a novel, first-in-class anti-secretory agent which has a basic normalizing effect locally on the gut, and this mechanism of action has the potential to benefit multiple disorders.


Lead Product(s): Crofelemer

Therapeutic Area: Gastroenterology Product Name: Mytesi

Highest Development Status: UndisclosedProduct Type: Small molecule

Recipient: Jaguar Health

Deal Size: $5.0 million Upfront Cash: Undisclosed

Deal Type: Agreement March 09, 2021

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Oasis agreed to purchase additional accounts receivable of the Company related to the sales of the Company's Mytesi® drug product to Cardinal Health for the period of August 11, 2020 through September 3, 2020.


Lead Product(s): Crofelemer

Therapeutic Area: Gastroenterology Product Name: Mytesi

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Oasis Capital

Deal Size: $2.3 million Upfront Cash: Undisclosed

Deal Type: Agreement September 10, 2020

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Under the the license, Jaguar has to initiate Phase 2 study of NP-500 under an investigational new drug application with the U.S. FDA or an IND-equivalent dossier within six months of April 15, 2020.


Lead Product(s): NP-500

Therapeutic Area: Endocrinology Product Name: Undisclosed

Highest Development Status: Phase IProduct Type: Undisclosed

Partner/Sponsor/Collaborator: Atlas Sciences

Deal Size: $1.5 million Upfront Cash: Undisclosed

Deal Type: Licensing Agreement April 16, 2020

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