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Protagonist Therapeutics Ranked in the Top 3% of Fastest-Growing Companies in North America on the 2023 Deloitte Technology Fast 500(TM)

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Protagonist Therapeutics (Nasdaq:PTGX) ranked in the top 3% of the 2023 Deloitte Technology Fast 500TM, showcasing impressive revenue growth fueled by a novel oral peptide therapeutic program. The company's CEO expressed pride in the recognition and highlighted the dedication of the team and strength of partnerships.
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  • Protagonist Therapeutics achieved significant revenue growth, validating their innovative peptide technology platform and promising peptide therapeutics.
  • The company's dedication to addressing unmet needs in patients through new medicines is commendable.
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NEWARK, CA / ACCESSWIRE / November 9, 2023 / Protagonist Therapeutics (Nasdaq:PTGX) today announced it ranked in the top 3% of the 2023 Deloitte Technology Fast 500TM, a list of the fastest-growing technology, media, telecommunications, life sciences, fintech and energy tech companies in North America. Life sciences and software companies dominated at the top of the Fast 500 this year; Protagonist joins Vir Biotechnology and Moderna among the top companies across all sectors.

The Deloitte Technology Fast 500 selects winners based on percentage fiscal year revenue growth from 2019 to 2022. Protagonist's revenue growth was fueled by milestones and royalties stemming from partnership of a novel oral peptide therapeutic program for immunologic and inflammatory disease.

Dinesh V. Patel, PhD, President and CEO, Protagonist Therapeutics, said, "Protagonist Therapeutics is very pleased to be ranked among the top 20 Deloitte Technology Fast 500 winners for 2023. This honor reflects the validation of our innovative peptide technology platform, the promise of peptide therapeutics, the dedication of our team and the strength of our partnerships. We intend to continue on this trajectory with the ultimate goal of bringing new medicines to address unmet needs in patients."

Paul Silverglate, vice chair, Deloitte LLP and U.S. technology sector leader, said, "Each year, we look forward to reviewing the progress and innovations of our Technology Fast 500 winners. This year is especially celebratory as we expand the number of winners to better represent just how many companies are developing new ideas to progress our society and the world, especially during a slow economy."

About the 2023 Deloitte Technology Fast 500TM

Now in its 29th year, the Deloitte Technology Fast 500 provides a ranking of the fastest-growing technology, media, telecommunications, life sciences, fintech, and energy tech companies - both public and private - in North America. Technology Fast 500 award winners are selected based on percentage fiscal year revenue growth from 2019 to 2022. In order to be eligible for Technology Fast 500 recognition, companies must own proprietary intellectual property or technology that is sold to customers in products that contribute to a majority of the company's operating revenues. Companies must have base-year operating revenues of at least US$50,000, and current-year operating revenues of at least US$5 million. Additionally, companies must be in business for a minimum of four years and be headquartered within North America.

About Protagonist Therapeutics

Protagonist Therapeutics is a biopharmaceutical company with peptide-based new chemical entities (NCEs) rusfertide and JNJ-2113 (formerly PN-235) in advanced stages of clinical development, both derived from the Company's proprietary technology platform. Protagonist and Janssen scientists jointly discovered PN-235 (now known as JNJ-2113) as part of Protagonist's Interleukin-23 receptor (IL-23R) collaboration with Janssen and followed it through IND-enabling pre-clinical and Phase 1 studies, with Janssen assuming responsibility for further clinical development. Rusfertide, a mimetic of the natural hormone hepcidin, is the Company's lead drug candidate currently in a global Phase 3 development program. The randomized portion of the Phase 2 REVIVE study was unblinded, showing positive results and is now complete, with an open-label extension underway. The global Phase 3 VERIFY study of rusfertide in polycythemia vera is ongoing. Protagonist retains all worldwide development and commercialization rights to rusfertide. More information on Protagonist, its pipeline drug candidates and clinical studies can be found on the Company's website at www.protagonist-inc.com.

Cautionary Note on Forward-Looking Statements

This press release contains forward-looking statements for purposes of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include statements regarding our proprietary peptide platform and our partnerships. In some cases, you can identify these statements by forward-looking words such as "anticipate," "believe," "may," "will," "expect," or the negative or plural of these words or similar expressions. Forward-looking statements are not guarantees of future performance and are subject to risks and uncertainties that could cause actual results and events to differ materially from those anticipated, including, but not limited to, our ability to develop and commercialize our product candidates, our ability to earn milestone payments under our collaboration agreement with Janssen, our ability to use and expand our programs to build a pipeline of product candidates, our ability to obtain and maintain regulatory approval of our product candidates, our ability to operate in a competitive industry and compete successfully against competitors that have greater resources than we do, and our ability to obtain and adequately protect intellectual property rights for our product candidates. Additional information concerning these and other risk factors affecting our business can be found in our periodic filings with the Securities and Exchange Commission, including under the heading "Risk Factors" contained in our most recently filed periodic reports on Form 10-K and Form 10-Q filed with the Securities and Exchange Commission. Forward-looking statements are not guarantees of future performance, and our actual results of operations, financial condition and liquidity, and the development of the industry in which we operate, may differ materially from the forward-looking statements contained in this press release. Any forward-looking statements that we make in this press release speak only as of the date of this press release. We assume no obligation to update our forward-looking statements, whether as a result of new information, future events or otherwise, after the date of this press release.

Media Contact
Virginia Amann, Founder/CEO
ENTENTE Network of Companies
virginiaamann@ententeinc.com

Investor Relations Contact
Corey Davis, Ph.D.
Lieske Advisors
+1 212 915 2577
cdavis@lifesciadvisors.com

SOURCE: Protagonist Therapeutics, Inc.



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FAQ

What is Protagonist Therapeutics (Nasdaq:PTGX) announcement about?

Protagonist Therapeutics ranked in the top 3% of the 2023 Deloitte Technology Fast 500TM, showcasing impressive revenue growth fueled by a novel oral peptide therapeutic program.

How does Deloitte Technology Fast 500 select winners?

Winners are selected based on percentage fiscal year revenue growth from 2019 to 2022.

What did Dinesh V. Patel, PhD, President and CEO, Protagonist Therapeutics, say about the ranking?

He expressed pride in the recognition and highlighted the dedication of the team and strength of partnerships.

Who is Paul Silverglate and what did he say about the 2023 Deloitte Technology Fast 500 winners?

Paul Silverglate is the vice chair, Deloitte LLP and U.S. technology sector leader. He mentioned that the expansion of the number of winners this year better represents the companies developing new ideas to progress society and the world, especially during a slow economy.

Protagonist Therapeutics, Inc.

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About PTGX

protagonist therapeutics is a clinical-stage biopharmaceutical company with a proprietary technology platform which is utilized to discover and develop novel peptide-based drugs to address significant unmet medical needs. its primary focus is on developing potential first-in-class oral targeted therapy-based peptide drugs that work by blocking biological pathways that are currently targeted by marketed injectable antibody drugs. protagonist's initial lead peptide product candidates, ptg-100 and ptg-200, are based on this approach, and the company believes these candidates have the potential to transform the existing treatment paradigm for inflammatory bowel disease (ibd), consisting primarily of ulcerative colitis and crohn's disease. ptg-100, a potential first-in-class oral peptide alpha-4-beta-7 integrin antagonist, is currently in a global phase 2b clinical trial for treatment of moderate-to-severe ulcerative colitis. ptg-200, a first-in-class oral interleukin-23 receptor antagonist