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Protagonist Therapeutics, Inc. Stock Price

NasdaqGM:PTGX Community·US$10.0b Market Cap
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PTGX Share Price Performance

US$154.32
97.44 (171.31%)
US$154.32
97.44 (171.31%)
Price US$154.32

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Snowflake Analysis

Flawless balance sheet with reasonable growth potential.

0 Risks
3 Rewards

Protagonist Therapeutics, Inc. Key Details

US$282.0m

Revenue

US$0

Cost of Revenue

US$282.0m

Gross Profit

US$199.1m

Other Expenses

US$82.9m

Earnings

Last Reported Earnings
Jun 30, 2026
Next Reporting Earnings
n/a
1.28
100.00%
29.40%
0%
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About PTGX

Founded
2006
Employees
141
CEO
Dinesh Patel
WebsiteView website
www.protagonist-inc.com

Protagonist Therapeutics, Inc. operates as a discovery and development company in the United States. It develops Icotyde, a first-in-class investigational targeted oral peptide for the treatment of adults and pediatric patients 12 years of age and older with moderate-to-severe plaque psoriasis; and Rusfertide, a first-in-class investigational injectable mimetic of the natural hormone hepcidin in Phase 3 development for the treatment of the rare blood disorder polycythemia vera. The company is also developing PN-881, a potential best-in-class oral peptide IL-17 antagonist, for the treatment of immune-mediated skin diseases in Phase 1 clinical trials; PN-477 and PN-458, which are development candidates for the treatment of obesity; PN-8047, an orally administered hepcidin functional mimetic small molecule; L-4R alpha antagonist for the treatment of atopic dermatitis and moderate-to-severe asthma; and amylinR-based oral and subcutaneous mono- and poly-agonists for the treatment of obesity. Protagonist Therapeutics, Inc. was incorporated in 2006 and is headquartered in Newark, California.

Recent PTGX News & Updates

Seeking Alpha Aug 12

Protagonist Therapeutics: 'Strong Buy' ICOTYDE FDA Approval And PN-881 Advancement

Summary Protagonist Therapeutics maintains a 'Strong Buy' rating, driven by FDA approval of ICOTYDE for moderate-to-severe plaque psoriasis and strong partnership economics. The company is advancing rusfertide for polycythemia vera, with an FDA Priority Review decision expected in August 2026 and substantial milestone and royalty potential from Takeda. The development pipeline includes the oral IL-17 antagonist PN-881 for psoriasis and other inflammatory disorders, with phase 2b study initiation planned for Q1 2027. A robust cash position of $849.5M and ongoing milestone/royalty streams support near-term operations and further clinical expansion. Read the full article on Seeking Alpha

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