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PTGXNasdaq

Protagonist Therapeutics, Inc

Biopharma developer (SEC filing verified)·Commercial·Newark, CA, United States·CEO: Dr. Dinesh V. Patel Ph.D.
OncologyImmunologyDermatology

PTGX evidence brief

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BioSniper AI · PTGX

Protagonist Therapeutics is a biopharmaceutical company focused on discovering and developing peptide-based therapies for hematology, immunology/inflammation, and metabolic diseases, with a lead product candidate rusfertide (for polycythemia vera) and a partnered oral IL-17 program.

Key risk: Dependence on partners

5.9/10

BioSniper Score

Based on 6 of 6 signals

Market Cap

$9.34B

Cash Runway

Lead Asset

Icotyde (BLA Filed)

Financial data as of Jun 30, 2026.

Tracking 2 pipeline candidates · 2 clinical trials · 1 catalyst for Protagonist Therapeutics, Inc.

AI OverviewAI overview is shown in English only.

Protagonist Therapeutics is a biopharmaceutical company focused on discovering and developing peptide-based therapies for hematology, immunology/inflammation, and metabolic diseases, with a lead product candidate rusfertide (for polycythemia vera) and a partnered oral IL-17 program.

  • As of June 30, 2026, Protagonist reported cash and equivalents of $420.4M, total revenue of $213.5M, net income of $162.8M, and shareholders' equity of $668.0M [sec].
  • The company's lead candidate, rusfertide, is being developed for polycythemia vera, and its commercialization depends on collaboration partners [sec_mda · as of 2026-08-05].
  • Protagonist has an oral IL-17 peptide antagonist program targeting three IL-17 dimers for conditions like hidradenitis suppurativa and plaque psoriasis [sec_mda · as of 2024-11-07].
  • The company's discovery pipeline focuses on hematology/blood disorders, immunology/inflammation (I&I) diseases, and metabolic diseases including obesity [sec_mda · as of 2024-11-07].
  • As of December 31, 2025, Protagonist had an accumulated deficit of $470.7 million [sec_mda · as of 2026-02-25].

What works

  • Protagonist has a strong cash position of $420.4M as of June 30, 2026, providing runway for ongoing development [sec].
  • The company achieved profitability in the latest reported period, with net income of $162.8M as of June 30, 2026 [sec].
  • The oral IL-17 program targets multiple dimers (AA, AF, FF) and could address large markets like hidradenitis suppurativa and psoriasis [sec_mda · as of 2024-11-07].

What to weigh

  • Protagonist has an accumulated deficit of $470.7 million as of December 31, 2025, indicating historical losses [sec_mda · as of 2026-02-25].
  • Commercialization of key assets like rusfertide and ICOTYDE depends on collaboration partners, limiting direct control [sec_mda · as of 2026-08-05].
  • The company may require additional funding to advance early discovery pipeline and in-license other candidates [sec_mda · as of 2025-11-06].

From the filings

Quoted directly from source documents.

  • Protagonist's cash position and accumulated deficit as of year-end 2025

    As of December 31, 2025, we had $646.0 million of cash, cash equivalents and marketable securities and an accumulated deficit of $470.7 million.

    SEC MD&A · February 25, 2026

  • The oral IL-17 program targets three IL-17 dimers for inflammatory diseases

    In January 2024, we announced a new oral Interleukin-17 ("IL-17") peptide antagonist program targeting three IL-17 dimers (IL-17 AA, AF and FF) which may offer potential treatment options for hidradenitis suppurativa, spondyloarthritis, plaque psoriasis and psoriatic arthritis.

    SEC MD&A · November 7, 2024

  • Commercialization of ICOTYDE and rusfertide depends on collaboration partners

    the commercialization of our product candidates, if approved, which for ICOTYDE and rusfertide depends largely on the efforts of our collaboration partners

    SEC MD&A · August 5, 2026

  • Protagonist's pipeline includes hematology, I&I, and metabolic diseases

    Our discovery pipeline has strategically focused on i) hematology and blood disorders, ii) I&I diseases and iii) metabolic diseases, including obesity.

    SEC MD&A · November 7, 2024

Catalyst timeline

  • 2041-11-19 · Patent_Expiry · ICOTYDE — Patent/Exclusivity Expiry: ICOTYDEThe patent/exclusivity expiry for ICOTYDE could affect market exclusivity and competitive positioning.
Risks & what to watch (4)

Key risks

  • Dependence on partnersCommercialization of rusfertide and ICOTYDE relies on collaboration partners, reducing control over timelines and revenue [sec_mda · as of 2026-08-05].
  • Clinical and regulatory uncertaintyForward-looking statements highlight risks in clinical trial enrollment, costs, and regulatory approvals [sec_mda · as of 2026-08-05].
  • Need for additional fundingProtagonist may require extra capital to advance early discovery and in-license candidates [sec_mda · as of 2025-11-06].
  • Accumulated deficitAs of December 31, 2025, the company had an accumulated deficit of $470.7 million [sec_mda · as of 2026-02-25].

What to watch

  • Progress of rusfertide clinical trials and regulatory submissions [sec_mda · as of 2026-08-05].
  • Advancement of the oral IL-17 program into IND-enabling studies [sec_mda · as of 2024-11-07].
  • Milestone payments and royalties from collaboration partners [sec_mda · as of 2026-08-05].
  • Patent expiry for ICOTYDE on November 19, 2041 [catalyst].

Sources: Catalysts · SEC MD&A · Generated August 27, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 6 of 6 signals · derived from public data

Cash Runway10.0

Profitable (positive operating cash flow)

Financial Health9.2

D/E 0.05 · 8% dilution

Pipeline Maturity9.5

Lead: BLA Filed

Pipeline Breadth4.6

2 candidates

Catalyst Momentum2.0

1 upcoming, next in ~5560d

Insider Signal0.0

0 buys · 16 sells (180d)

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

320

Total value held

$8.15B

HolderSharesValue
blackrock, inc.9,779,369$1.03B
farallon capital management llc6,348,906$669.2M
janus henderson group plc5,783,054$609.7M
rtw investments, lp5,059,053$533.2M
wellington management group llp3,599,644$379.4M
vanguard portfolio management llc3,481,211$366.9M
state street corp3,116,749$328.5M
woodline partners lp2,828,346$298.1M
vanguard capital management llc2,805,896$295.7M
perceptive advisors llc2,461,758$259.5M

Showing top 10 of 320 institutional holders of Protagonist Therapeutics, Inc. Open the full 13F history after sign-in.

Short Interest

as of May 22, 2026
% of float
13.6%
Days to cover
10.7
Shares short
7,540,996
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

PTGX short interest

Governance

Frequently asked questions

What is the AI investment thesis for Protagonist Therapeutics, Inc?

Protagonist Therapeutics is a biopharmaceutical company focused on discovering and developing peptide-based therapies for hematology, immunology/inflammation, and metabolic diseases, with a lead product candidate rusfertide (for polycythemia vera) and a partnered oral IL-17 program.

What is Protagonist Therapeutics, Inc's lead drug candidate?

Protagonist Therapeutics, Inc's most advanced tracked candidate is Icotyde (BLA Filed) for Moderate-to-severe plaque psoriasis, psoriatic arthritis, inflammatory bowel disease.

What is Protagonist Therapeutics, Inc's next catalyst?

Protagonist Therapeutics, Inc's next tracked catalyst is a Patent_Expiry event — "Patent/Exclusivity Expiry: ICOTYDE" — expected November 19, 2041.

Who is the CEO of Protagonist Therapeutics, Inc?

Dr. Dinesh V. Patel Ph.D. is the chief executive officer of Protagonist Therapeutics, Inc (PTGX).

Where is Protagonist Therapeutics, Inc headquartered?

Protagonist Therapeutics, Inc (PTGX) is headquartered in Newark, CA, United States.

925 companies232,681 SEC filings21,419 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.