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KYNBNasdaq

KYNTRA BIO INC.

Biopharma developer (SEC filing verified)·Commercial·San Francisco, CA, United States·CEO: Mr. Thane Wettig
OncologyRare DiseaseNeurologyImmunologyCardiovascularMetabolicHematologyNephrology

KYNB evidence brief

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BioSniper AI · KYNB

Kyntra Bio Inc. (KYNB) is a biopharmaceutical company focused on developing therapies for anemia and oncology, with commercial sales of roxadustat in Japan and Europe and a pipeline including FG-3246 in Phase 2.

Key risk: Continued operating losses

7.6/10

BioSniper Score

Based on 6 of 6 signals

Market Cap

$32.5M

Cash Runway

68.4 mo

Lead Asset

EVRENZO (爱瑞卓®) / roxadustat (Approved)

Financial data as of Jun 30, 2026.

Tracking 4 pipeline candidates · 128 clinical trials · 15 catalysts for KYNTRA BIO INC..

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AI OverviewAI overview is shown in English only.

Kyntra Bio Inc. (KYNB) is a biopharmaceutical company focused on developing therapies for anemia and oncology, with commercial sales of roxadustat in Japan and Europe and a pipeline including FG-3246 in Phase 2.

  • Cash and equivalents of $50.6M as of 2026-06-30 [sec].
  • Net income of $12.0M for the period ended 2026-06-30 [sec].
  • Commercial sales of roxadustat in Japan and Europe generate revenue [sec_mda · as of 2026-08-13].
  • FG-3246 is in Phase 2 clinical development [sec_mda · as of 2026-05-12].
  • The company has incurred approximately $3.3 billion in cumulative R&D expenses through December 31, 2025 [sec_mda · as of 2026-03-16].

What works

  • Kyntra Bio has a commercial product, roxadustat, generating revenue in Japan and Europe [sec_mda · as of 2026-08-13].
  • The company successfully monetized its China business for $220M, exceeding expectations and repaying debt [sec · filed 2026-04-27].
  • Research and development expenses have decreased due to a cost reduction plan implemented in the U.S. in Q3 2024 [sec_mda · as of 2026-03-16].

What to weigh

  • The company anticipates continued losses for the foreseeable future despite roxadustat revenue [sec_mda · as of 2026-08-13].
  • Substantial additional funding will be needed to support ongoing operations and development [sec_mda · as of 2026-03-16].
  • Cumulative R&D expenses total approximately $3.3 billion, with no guarantee of future product success [sec_mda · as of 2026-03-16].
  • The company is subject to all risks associated with developing and commercializing novel therapeutics [sec_mda · as of 2026-03-16].

From the filings

Quoted directly from source documents.

  • Revenue from roxadustat in Japan and Europe

    We generate revenue from commercial sales of roxadustat product in Japan and Europe.

    SEC MD&A · August 13, 2026

  • Cumulative R&D expenses through December 31, 2025

    Since inception and through December 31, 2025, we have incurred a total of approximately $3.3 billion in research and development expenses

    SEC MD&A · March 16, 2026

Catalyst timeline

  • 2026-12-01 · Phase3_Topline — ProBioTopline data from the Phase 3 ProBio study in metastatic cancer will be reported.
  • 2027-09-01 · Phase3_Topline · enzalutamide — CASPARTopline data from the Phase 3 CASPAR trial of enzalutamide and rucaparib in first-line metastatic disease will be reported.
  • 2027-12-01 · Phase3_Topline — Apa/Enza Short StudyTopline data from the Phase 3 study of shortened androgen receptor signaling agent duration will be reported.
  • 2027-12-15 · Phase3_Topline · jnt-517Topline data from the Phase 3 double-blind, randomized study of JNT-517 will be reported.
Risks & what to watch (4)

Key risks

  • Continued operating lossesThe company expects to continue generating losses for the foreseeable future despite roxadustat revenue [sec_mda · as of 2026-08-13].
  • Need for additional fundingSubstantial additional funding will be required to support ongoing operations and development [sec_mda · as of 2026-03-16].
  • Clinical development risksThe company faces all risks inherent in developing and commercializing novel therapeutics, including unforeseen delays and expenses [sec_mda · as of 2026-03-16].
  • Dependence on pipeline successNo guarantee that sufficient funds will be available to fund development through commercialization [sec_mda · as of 2026-08-13].

What to watch

  • Phase 3 topline results for ProBio study expected December 2026 [upcoming catalysts].
  • Phase 3 topline results for CASPAR trial (enzalutamide + rucaparib) expected September 2027 [upcoming catalysts].
  • Phase 3 topline results for Apa/Enza Short study expected December 2027 [upcoming catalysts].
  • Phase 3 topline results for JNT-517 study expected December 2027 [upcoming catalysts].

Sources: SEC filings · SEC MD&A · Generated August 29, 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

68.4 months

Financial Health2.0

OCF -$4M · Net income $12M

Pipeline Maturity10.0

Lead: Approved

Pipeline Breadth7.2

4 candidates

Catalyst Momentum10.0

15 upcoming, next in ~93d

Insider Signal6.5

1 buy · 0 sells (180d)

Runway

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

31

Total value held

$7.5M

Showing top 10 of 31 institutional holders of KYNTRA BIO INC.. Open the full 13F history after sign-in.

Short Interest

as of Apr 19, 2026
% of float
2.9%
Days to cover
3.2
Shares short
113,876
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 →

KYNB short interest

Governance

Frequently asked questions

What is the AI investment thesis for KYNTRA BIO INC.?

Kyntra Bio Inc. (KYNB) is a biopharmaceutical company focused on developing therapies for anemia and oncology, with commercial sales of roxadustat in Japan and Europe and a pipeline including FG-3246 in Phase 2.

What is KYNTRA BIO INC.'s lead drug candidate?

KYNTRA BIO INC.'s most advanced tracked candidate is EVRENZO (爱瑞卓®) / roxadustat (Approved) for Myelodysplastic Syndromes.

What is KYNTRA BIO INC.'s next catalyst?

KYNTRA BIO INC.'s next tracked catalyst is a Phase3_Topline event — "Phase 3 Topline: ProBio: An Outcome-adaptive and Randomized Multi-arm Biomarker Driven Study in Patients With Metasta" — expected December 1, 2026.

Who is the CEO of KYNTRA BIO INC.?

Mr. Thane Wettig is the chief executive officer of KYNTRA BIO INC. (KYNB).

Where is KYNTRA BIO INC. headquartered?

KYNTRA BIO INC. (KYNB) is headquartered in San Francisco, 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.