Portola Pharmaceuticals

Last updated

Portola Pharmaceuticals
Company type Public [1]
Industry Pharmaceuticals
Founded2003
FoundersCharles J. Homcy, David R. Philips
FateAcquired by Alexion Pharmaceuticals
Headquarters South San Francisco, California, United States
Area served
Worldwide
Key people
Scott Garland (CEO) [1]
Products Andexxa
Bevyxxa
Cerdulatinib
Revenue$40,130 (2018) [1]
Number of employees
324 (2018) [1]
Subsidiaries Portola Pharma UK Limited
Website portola.com

Portola Pharmaceuticals is an American clinical stage biotechnology company that researches, develops, and commercializes drugs. The company focuses primarily on drugs used in the treatment of thrombosis and hematological malignancies. [2] Founded in 2003 and headquartered in South San Francisco, California, Portola Pharmaceuticals is a member of the NASDAQ Biotechnology Index.

Contents

In May 2020, Alexion Pharmaceuticals and Portola announced that they had entered into a definitive merger agreement for Alexion to acquire Portola. [3]

History

The company was founded on September 2, 2003, [4] and named after Gaspar de Portolà, who was the first European to see San Francisco Bay. It completed an IPO on NASDAQ in May 2013. [5]

The company developed P2Y12 inhibitor Elinogrel, transferring rights to Novartis in 2009. [6] The rights were returned in 2012 to Portola, which decided not to continue development.

Portola Pharmaceuticals has collaboration agreements with SRX Cardio, Dermavant, Millennium Pharmaceuticals, Daiichi Sankyo, Bayer, Janssen, BMS, and Pfizer. [7]

In the class action lawsuit of Hayden v. Portola Pharmaceuticals in U.S. District Court, in the Northern District of California, before U.S. District Judge Vince Chhabria, plaintiffs sued under Section 11 of the Securities Act of 1933 alleging that the company and its underwriters misrepresented its financial position ahead of a 2019 securities offering. [8] [9] In November 2022, Judge Chhabria entered an order granting preliminary approval of the proposed settlement of the case in the proposed settlement amount of $17.5 million. [10] [11] [12]

Products

Related Research Articles

<span class="mw-page-title-main">Anticoagulant</span> Class of drugs

An anticoagulant, commonly known as a blood thinner, is a chemical substance that prevents or reduces coagulation of blood, prolonging the clotting time. Some of them occur naturally in blood-eating animals such as leeches and mosquitoes, where they help keep the bite area unclotted long enough for the animal to obtain some blood.

<span class="mw-page-title-main">Rivaroxaban</span> Anticoagulant drug

Rivaroxaban, sold under the brand name Xarelto among others, is an anticoagulant medication used to treat and prevent blood clots. Specifically it is used to treat deep vein thrombosis and pulmonary emboli and prevent blood clots in atrial fibrillation and following hip or knee surgery. It is taken by mouth.

Eculizumab, sold under the brand name Soliris among others, is a recombinant humanized monoclonal antibody used to treat paroxysmal nocturnal hemoglobinuria (PNH), atypical hemolytic uremic syndrome (aHUS), generalized myasthenia gravis, and neuromyelitis optica. In people with PNH, it reduces both the destruction of red blood cells and need for blood transfusion, but does not appear to affect the risk of death. Eculizumab was the first drug approved for each of its uses, and its approval was granted based on small trials. It is given by intravenous infusion.

Direct factor Xa inhibitors (xabans) are anticoagulants, used to both treat and prevent blood clots in veins, and prevent stroke and embolism in people with atrial fibrillation (AF).

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<span class="mw-page-title-main">Betrixaban</span> Chemical compound

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<span class="mw-page-title-main">Elinogrel</span> Chemical compound

Elinogrel (INN, USAN) was an experimental antiplatelet drug acting as a P2Y12 inhibitor. Similarly to ticagrelor and in contrast to clopidogrel, elinogrel was a reversible inhibitor that acted fast and short (for about 12 hours), and it was not a prodrug but pharmacologically active itself. The substance was used in form of its potassium salt, intravenously for acute treatment and orally for long-term treatment. Development was terminated in 2012.

<span class="mw-page-title-main">Ruxolitinib</span> Medication

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<span class="mw-page-title-main">Apixaban</span> Anticoagulant medication

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Andexanet alfa, sold under the brand name Andexxa among others, is an antidote for the medications rivaroxaban and apixaban, when reversal of anticoagulation is needed due to uncontrolled bleeding. It has not been found to be useful for other factor Xa inhibitors. It is given by injection into a vein.

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References

  1. 1 2 3 4 "FORM 10-K For the Fiscal Year Ended December 31, 2018". portola.com. Retrieved May 13, 2019.
  2. "Corporate site". portola.com. Retrieved May 11, 2019.
  3. Alexion to Acquire Portola, businesswire.com, Retrieved 5 May 2020.
  4. "EX-3.2". sec.gov.
  5. "Portola Pharmaceuticals prices upsized IPO at $14.50, within the range"
  6. "Novartis gains worldwide rights to elinogrel, a Phase II anti-clotting compound". pharmanews.eu. Retrieved November 3, 2018.
  7. "Collaborations, Portola Website" . Retrieved May 11, 2019.
  8. Godoy, Jody (August 11, 2021). "Portola Pharmaceuticals, underwriters lose bid to toss shareholder lawsuit". Reuters via reuters.com.
  9. "Judge Dismisses Securities Claims As Lacking In Drug Company's Stock-Drop Suit - Lexis Legal News". lexislegalnews.com.
  10. "REMOTE HEARINGS". apps.cand.uscourts.gov.
  11. "Securities Settlement Approved in Class Action Against Portola Pharmaceuticals | Law Street Media". November 1, 2022.
  12. https://www.bermantabacco.com/wp-content/uploads/2022/12/portolapharmaceuticals-notice.pdf
  13. "FDA Approval Letter - ANDEXXA, May 3, 2018". fda.gov. Retrieved May 11, 2019.
  14. "EMA Positive Opinion - ONDEXXYA, March 1, 2019". ema.europa.eu. Retrieved May 11, 2019.
  15. "European Commission Grants Conditional Marketing Authorization for Portola Pharmaceuticals' Ondexxya™ (andexanet alfa), the First and Only Antidote for the Reversal of Factor Xa Inhibitors, PM Portola, April 26, 2019". portola.com. Retrieved May 11, 2019.
  16. "FDA approved betrixaban (BEVYXXA, Portola) for the prophylaxis of venous thromboembolism (VTE) in adult patients, FDA, June 23, 2017". fda.gov. November 3, 2018. Retrieved May 11, 2019.
  17. "NASDAQ: Portola's (PTLA) Lymphoma Candidate Gets Orphan Drug Status, September 26, 2018". nasdaq.com. Retrieved May 11, 2019.