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ZURANasdaq

Zura Bio Ltd

Biopharma developer (SEC filing verified)·Phase 2·Henderson, NV, United States·CEO: Dr. Sandeep Chidambar Kulkarni M.D.
ImmunologyRespiratoryDermatology

ZURA evidence brief

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Prepared research question

What matters most for ZURA—catalysts, financial risk and supporting evidence?

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BioSniper AI · ZURA

Zura Bio Ltd is a clinical-stage biotechnology company developing tibulizumab, a bispecific antibody targeting autoimmune and inflammatory diseases, with no approved products or revenue to date.

Key risk: No revenue or approved products

6.0/10

BioSniper Score

Based on 5 of 6 signals

Market Cap

$548.1M

Cash Runway

Lead Asset

crebankitug (Preclinical)

Financial data as of Jun 30, 2026.

Tracking 3 pipeline candidates · 2 clinical trials · 1 catalyst for Zura Bio Ltd.

AI OverviewAI overview is shown in English only.

Zura Bio Ltd is a clinical-stage biotechnology company developing tibulizumab, a bispecific antibody targeting autoimmune and inflammatory diseases, with no approved products or revenue to date.

  • Zura Bio has no approved products and has not generated any revenue from commercial sales [sec_mda · as of 2026-08-11].
  • Cash and cash equivalents were $0.2M as of June 30, 2026, with a net loss of $26.3M for the six months ended June 30, 2026 [sec].
  • The company expects existing cash to fund operations through at least the end of 2028, based on current business plans [sec_mda · as of 2026-08-11].
  • Tibulizumab is in Phase 2 trials for autoimmune and inflammatory diseases, with topline data expected by the end of 2026 [catalyst].
  • Zura Bio is obligated to pay milestone payments and royalties to Pfizer and Lilly under licensing agreements [sec_mda · as of 2026-08-11].

What works

  • Zura Bio has a clear near-term catalyst with the expected Phase 2 topline readout for tibulizumab by the end of 2026 [catalyst].
  • The company believes its existing cash will fund operations through at least the end of 2028, providing a runway for key development milestones [sec_mda · as of 2026-08-11].

What to weigh

  • Zura Bio has no approved products or revenue and expects to continue incurring significant operating losses for the foreseeable future [sec_mda · as of 2026-08-11].
  • Cash and cash equivalents were only $0.2M as of June 30, 2026, indicating a need for additional financing to sustain operations beyond the current runway [sec].
  • The company faces substantial milestone payment obligations to Pfizer and Lilly, which may become due before any product revenue is generated [sec_mda · as of 2026-08-11].

From the filings

Quoted directly from source documents.

  • Zura Bio has no approved products and no revenue.

    Since our inception, we have not reached successful commercialization of our product candidates or generated any revenue

    SEC MD&A · August 11, 2026

  • Cash runway is expected through at least the end of 2028.

    we believe that our existing cash and cash equivalents should be sufficient to fund our operating expenses and capital requirements through at least the end of 2028

    SEC MD&A · August 11, 2026

  • Tibulizumab Phase 2 topline data expected by end of 2026.

    Phase2_Topline: Phase 2 Readout: tibulizumab - Expected Phase 2 topline data readout for tibulizumab in autoimmune and inflammatory diseases

    Catalysts · December 31, 2026

  • Milestone and royalty obligations to Pfizer and Lilly.

    We will be required to pay certain of these milestone payments prior to the time at which we are able to generate sufficient revenue, if any, from commercial sales of any of our product candidates

    SEC MD&A · August 11, 2026

Catalyst timeline

  • 2026-12-31 · Phase2_Topline · tibulizumab — Phase 2 Readout: tibulizumabExpected topline data from Phase 2 trial of tibulizumab in autoimmune and inflammatory diseases, a key value inflection point.
Risks & what to watch (4)

Key risks

  • No revenue or approved productsZura Bio has no commercial products and no revenue, relying entirely on future development success [sec_mda · as of 2026-08-11].
  • Limited cash runwayCash of $0.2M as of June 30, 2026, may require additional financing before the end of 2028 [sec].
  • Milestone payment obligationsMultimillion-dollar milestone payments to Pfizer and Lilly are due before any product revenue, straining finances [sec_mda · as of 2026-08-11].
  • Clinical development riskTibulizumab is in Phase 2 and may fail to meet endpoints, delaying or preventing regulatory approval [catalyst].

What to watch

  • Phase 2 topline data for tibulizumab expected by end of 2026 [catalyst].
  • Any additional financing or equity offerings to extend cash runway [sec_mda · as of 2026-08-11].
  • Progress of ongoing Phase 2 trials for tibulizumab in autoimmune indications [catalyst].

Sources: Catalysts · SEC MD&A · Generated August 18, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 5 of 6 signals · derived from public data

Cash Runway10.0

Profitable (positive operating cash flow)

Financial Health5.0

OCF $19M · Net income -$26M

Pipeline Maturity6.0

Lead: Phase 2

Pipeline Breadth5.9

3 candidates

Catalyst Momentum3.0

1 upcoming, next in ~123d

Insider SignalN/A

No insider transactions in the last 180 days

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

89

Total value held

$296.5M

Showing top 10 of 89 institutional holders of Zura Bio Ltd. Open the full 13F history after sign-in.

Short Interest

as of May 22, 2026
% of float
9.9%
Days to cover
11.2
Shares short
6,974,577
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 →

ZURA short interest

Governance

Frequently asked questions

What is the AI investment thesis for Zura Bio Ltd?

Zura Bio Ltd is a clinical-stage biotechnology company developing tibulizumab, a bispecific antibody targeting autoimmune and inflammatory diseases, with no approved products or revenue to date.

What is Zura Bio Ltd's lead drug candidate?

Zura Bio Ltd's most advanced tracked candidate is crebankitug (Preclinical) for Autoimmune diseases where IL-7 or TSLP signaling has been implicated.

What is Zura Bio Ltd's next catalyst?

Zura Bio Ltd's next tracked catalyst is a Phase2_Topline event — "Phase 2 Readout: tibulizumab" — expected December 31, 2026.

Who is the CEO of Zura Bio Ltd?

Dr. Sandeep Chidambar Kulkarni M.D. is the chief executive officer of Zura Bio Ltd (ZURA).

Where is Zura Bio Ltd headquartered?

Zura Bio Ltd (ZURA) is headquartered in Henderson, NV, 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.