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BYSI

BeyondSpring Inc.

Pharmaceutical preparations·Phase 3·Florham Park, NJ, United States·CEO: Mr. Min Qiu
Oncology

BYSI evidence brief

What we can confirm

BioSniper Score:
4.6 / 10
Market Cap:
$32.0M
Lead Asset:
Plinabulin (Phase 3)

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $32.0M · Lead Asset: Plinabulin (Phase 3)
BioSniper AIPage evidence connected

Prepared research question

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

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · BYSI

BeyondSpring Inc. (BYSI) is a clinical-stage biotech focused on plinabulin, a microtubule-binding agent for non-small cell lung cancer, with a recent FDA Fast Track designation and a strategic transaction for the asset.

Key risk: Low cash runway

4.6/10

BioSniper Score

Based on 3 of 6 signals

Limited data coverage

Market Cap

$32.0M

Cash Runway

—

Lead Asset

Plinabulin (Phase 3)

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 1 pipeline candidate · 1 clinical trial for BeyondSpring Inc..

Similar companies

AI OverviewAI overview is shown in English only.

BeyondSpring Inc. (BYSI) is a clinical-stage biotech focused on plinabulin, a microtubule-binding agent for non-small cell lung cancer, with a recent FDA Fast Track designation and a strategic transaction for the asset.

  • Lead candidate plinabulin is in Phase 3 for non-small cell lung cancer as a selective immunomodulating microtubule-binding agent [pipeline].
  • Cash & equivalents were $2.7M as of 2026-06-30, with zero revenue and a net loss of $0.8M for the period [sec].
  • FDA granted Fast Track designation for plinabulin in post-ICI non-squamous NSCLC as of September 2026 [news · published 2026-09-29].
  • ASCO 2026 data showed a long-term survival benefit of plinabulin/docetaxel and pembrolizumab in metastatic NSCLC after progression on first-line ICI therapy [news · published 2026-08-14].
  • AACR 2026 preclinical data positioned plinabulin as a potential backbone agent to combine with ADC regimens [news · published 2026-05-13].

What works

  • Plinabulin has completed a Phase 3 trial (DUBLIN-3) showing a statistically significant median OS improvement (10.5 vs 9.4 months, p=0.0399) [catalyst].
  • The company has secured FDA Fast Track designation for plinabulin in a specific NSCLC indication, which may expedite development and review [news · published 2026-09-29].
  • Preclinical data suggest plinabulin could be combined with ADC therapies, potentially broadening its application [news · published 2026-05-13].

What to weigh

  • Cash position is very low at $2.7M as of 2026-06-30, with no revenue and a negative shareholders' equity of -$35.6M [sec].
  • The company reported a net loss of $0.8M for the period ending 2026-06-30, indicating ongoing cash burn without product revenue [sec].
  • Plinabulin faces competition from PD-1/PD-L1 antibodies, ADCs, and docetaxel in the NSCLC space [pipeline].
  • The Phase 3 OS benefit, while statistically significant, was modest (1.1 months median improvement) [catalyst].

From the filings

Quoted directly from source documents.

  • Plinabulin is a selective immunomodulating microtubule-binding agent in Phase 3 for NSCLC

    “Pipeline Candidate: Plinabulin Generic Name: Plinabulin Indication: Non-Small Cell Lung Cancer Phase: Phase 3 Mechanism of Action: Selective Immunomodulating Microtubule-Binding Agent (SIMBA) that depolymerizes microtubules, activates GEF-H1, and induces dendritic cell maturation”

    Pipeline

  • Phase 3 DUBLIN-3 trial showed a median OS of 10.5 vs 9.4 months (p=0.0399)

    “Median OS was 10·5 months (95% CI 9·34-11·87) in the plinabulin group compared with 9·4 months (8·38-10·68) in the control group (stratified HR 0·82, 95% CI 0·68-0·99; p=0·0399).”

    Catalysts · October 31, 2024

  • FDA Fast Track designation for plinabulin in post-ICI non-squamous NSCLC

    “BeyondSpring Inc. (BYSI) Discusses FDA Fast Track Designation and Strategic Transaction for Plinabulin in Post-ICI Non-Squamous NSCLC”

    News · September 29, 2026

Catalyst timeline

  • 2024-10-31 · Trial_Readout: Plinabulin plus docetaxel versus docetaxel in patients with non-small-cell lung cancer after disease progression on platinum-based regimen (DUBLIN-3): a phase 3, international, multicentre, single-blind, parallel group, randomised controlled trial. — Phase 3 readout showed a statistically significant but modest median OS improvement of 1.1 months.
Risks & what to watch (4)›

Key risks

  • Low cash runway — Cash of $2.7M as of 2026-06-30 with no revenue and a net loss of $0.8M suggests limited operating runway [sec].
  • Negative shareholders' equity — Shareholders' equity was -$35.6M as of 2026-06-30, indicating accumulated losses exceed capital [sec].
  • Modest Phase 3 OS benefit — Median OS improvement of 1.1 months in DUBLIN-3 may limit commercial differentiation vs competitors [catalyst].
  • Competitive landscape — Plinabulin competes with PD-1/PD-L1 antibodies, ADCs, and docetaxel in NSCLC [pipeline].

What to watch

  • Outcome of the strategic transaction for plinabulin discussed in September 2026 [news · published 2026-09-29].
  • Next clinical readouts from plinabulin combination studies with ADCs or pembrolizumab [news · published 2026-08-14].
  • Cash position updates in future quarterly filings to assess runway [sec].
  • Any regulatory milestones following the Fast Track designation [news · published 2026-09-29].

Sources: Catalysts · Competitor trials · News · Pipeline · Generated October 12, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 3 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health2.0

Net income -$849K

Pipeline Maturity8.5

Lead: Phase 3

Pipeline Breadth3.3

1 candidate

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider SignalN/A

No insider transactions in the last 180 days

Pipeline

Regulatory

Financials

Short Interest

as of May 20, 2026
% of float
6.4%
Days to cover
224.7
Shares short
2,188,849
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 →

BYSI short interest

Frequently asked questions

What is the AI investment thesis for BeyondSpring Inc.?

BeyondSpring Inc. (BYSI) is a clinical-stage biotech focused on plinabulin, a microtubule-binding agent for non-small cell lung cancer, with a recent FDA Fast Track designation and a strategic transaction for the asset.

What is BeyondSpring Inc.'s lead drug candidate?

BeyondSpring Inc.'s most advanced tracked candidate is Plinabulin (Phase 3) for Non-Small Cell Lung Cancer.

Who is the CEO of BeyondSpring Inc.?

Mr. Min Qiu is the chief executive officer of BeyondSpring Inc. (BYSI).

Where is BeyondSpring Inc. headquartered?

BeyondSpring Inc. (BYSI) is headquartered in Florham Park, NJ, United States.

What therapeutic areas does BeyondSpring Inc. focus on?

BeyondSpring Inc. develops therapies across Oncology.

923 companies304,844 SEC filings22,644 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.