STOCK TITAN

BeyondSpring Reports Second-Quarter 2026 Financial Results and Provides Corporate Update

(Very Positive)
Tags

BeyondSpring (NASDAQ: BYSI) reported second-quarter 2026 results and highlighted new clinical and leadership developments around its lead asset, Plinabulin. Updated ASCO 2026 Phase 2 data in metastatic NSCLC post-ICI showed median progression-free survival of 7.0 months, median duration of response of 9.3 months, disease control rate of 79.5%, and a 24‑month overall survival rate of 58.0%, with median overall survival not yet reached.

AACR 2026 preclinical data indicated that Plinabulin improved complete tumor regression, survival and tolerability when combined with certain TOP1-based ADCs. The company is preparing the 442‑patient confirmatory DUBLIN‑4 Phase 3 study. Q2 2026 R&D and G&A expenses were $1.0 million and $0.8 million, respectively, net loss from continuing operations was $1.8 million, and cash, cash equivalents and short-term investments totaled $6.5 million at June 30, 2026. A leadership transition effective July 1, 2026 installed Min Qiu as CEO and Na Li as CFO.

Loading...
Loading translation...

Positive

  • ASCO Phase 2 OS rate at 24 months 58.0%
  • Median PFS and DOR of 7.0 and 9.3 months in NSCLC post‑ICI
  • Disease control rate 79.5% in 47‑patient Phase 2 NSCLC study
  • Q2 2026 G&A expenses down to $0.8 million from $0.9 million
  • Six‑month 2026 net loss from continuing operations improved to $4.1 million from $4.5 million
  • Planned 442‑patient DUBLIN‑4 confirmatory Phase 3 trial in NSCLC

Negative

  • No revenue reported in Q2 2026 from continuing operations
  • Cash, cash equivalents and short‑term investments fell to $6.5 million from $12.6 million
  • Total liabilities of $50.6 million exceed total assets of $14.6 million
  • Q2 2026 net loss from continuing operations $1.8 million
  • Shareholders’ deficit widened to $36.0 million at June 30, 2026
  • Current liabilities $14.2 million exceed current assets of $9.9 million

News Explained

DUBLIN-4 remains planned, while financing is only being prepared; no raise, proceeds, or dilution is committed by this release.

BeyondSpring describes DUBLIN-4 as a planned 442-patient Phase 3 study and says financing preparations are needed to initiate it; this release announces no financing terms or completed raise, so it commits neither new shares nor financing proceeds.

Under the supplied definition, issuing additional shares would increase the total share count and reduce existing holders’ percentage ownership absent offsetting changes; the release does not state that such issuance has occurred.

At March 31, 2026, cash and equivalents were $4,036,000 and first-quarter operating cash outflow was $3,277,000; that balance equals 110.8 days of the reported operating cash use.

Sources and calculations
  • Cash and equivalents vs quarterly operating cash outflow, in days of cash use $4,036,000 / ($3,277,000 / 90) = [object Object]

Market Context

The prior earnings record averaged 1.63% across five tag-matched events, spanning aligned and diverg...
Analysis

The prior earnings record averaged 1.63% across five tag-matched events, spanning aligned and divergent responses. This release paired Phase 2 survival data with reduced cash; DUBLIN-4 execution and financing preparations were the key areas to watch.

Key Figures

Sample Size: 47 patients Median PFS: 7.0 months Disease Control Rate: 79.5% +5 more
8 metrics
Sample Size 47 patients Phase 2 Study 303 in metastatic NSCLC
Median PFS 7.0 months Phase 2 Study 303
Disease Control Rate 79.5% Phase 2 Study 303
Objective Response Rate 18.2% Confirmed rate in Phase 2 Study 303
24-Month Overall Survival 58.0% Phase 2 Study 303
DUBLIN-4 Enrollment 442 patients Planned confirmatory Phase 3 study
Net Loss $1.8 million Quarter ended June 30, 2026
Cash and Investments $6.5 million As of June 30, 2026, versus $12.6 million as of December 31, 2025

Previous Earnings Reports

5 past events · Latest: May 13 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 13 Q1 earnings report Positive +4.3% Pipeline updates and reduced continuing-operations loss preceded a 4.32% positive reaction.
Mar 25 2025 earnings report Positive +3.7% Phase 3 efficacy and strategic progress preceded a 3.7% positive reaction.
Nov 12 Q3 earnings report Positive -3.6% Clinical data and corporate milestones accompanied a 3.64% negative reaction.
Aug 13 Q2 earnings report Neutral -0.5% Clinical advances and leadership appointment accompanied a 0.5% negative reaction.
May 12 Q1 earnings report Negative +4.3% Higher expenses and continuing-operations loss preceded a 4.25% positive reaction.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

The five tag-specific earnings events averaged a 1.63% move, with two aligned reactions and three divergences.

Key Terms

nsclc, immune checkpoint inhibitor, progression-free survival, antibody-drug conjugates
4 terms
nsclc medical
"in metastatic NSCLC patients whose disease progressed after first-line immune checkpoint inhibitor"
NSCLC stands for non-small cell lung cancer, which is the most common type of lung cancer. It develops in the lungs and can spread to other parts of the body, making it serious but often treatable if caught early. Understanding NSCLC helps people recognize the importance of lung health and early detection.
immune checkpoint inhibitor medical
"after first-line immune checkpoint inhibitor (ICI) therapy"
An immune checkpoint inhibitor is a type of medicine that helps the body's immune system recognize and attack cancer cells more effectively. It works by blocking certain signals that cancer uses to hide from immune defenses, allowing the immune system to target tumors. This breakthrough has led to new cancer treatments, making immune checkpoint inhibitors an important area of growth and innovation in the healthcare industry.
progression-free survival medical
"median progression-free survival was 7.0 months"
Progression-free survival is the length of time during and after a treatment that a patient's disease does not get worse, measured from the start of treatment until the disease shows measurable signs of progression or the patient dies. Investors care because longer progression-free survival in clinical trials often signals that a drug is effective, improving chances of regulatory approval, market adoption, and revenue potential—think of it as a stopwatch showing how long a therapy can keep the illness at bay.
antibody-drug conjugates medical
"combination with the approved topoisomerase I inhibitor (TOP1)-based ADCs"
A class of targeted cancer medicines that combine a lab-made antibody (which finds and sticks to specific markers on tumor cells) with a powerful cell-killing drug linked together so the toxic payload is delivered directly to the tumor. Think of it like a guided missile that reduces collateral damage compared with traditional chemotherapy; for investors, success or failure of these drugs drives clinical, regulatory and commercial value and can sharply affect a biotech company’s prospects and stock price.

AI-generated analysis. How Rhea-AI works. Not financial advice.

See more from StockTitan in Google Search and AI answers. Adds StockTitan as a preferred source · opens Google
Add on Google

ASCO 2026 Data Demonstrate Long-term Survival Benefit of Plinabulin/Docetaxel and Pembrolizumab in Metastatic NSCLC Following Progression on First-Line Immune Checkpoint Inhibitor (ICI) Therapy

AACR 2026 Preclinical Data Provide the Scientific Rationale for Plinabulin as a Potential Backbone Agent to Combine with Antibody-Drug Conjugate (ADC) Regimens to Improve Efficacy, Survival and Tolerability

Leadership Transition Effective July 1, 2026 Aligns the Organization Around Focused Advancement of the Confirmatory DUBLIN-4 Program in NSCLC Post-ICI and Long-Term Value Creation

FLORHAM PARK, N.J., Aug. 14, 2026 (GLOBE NEWSWIRE) -- BeyondSpring Inc. (NASDAQ: BYSI) (“BeyondSpring” or the “Company”), a clinical-stage company developing transformative therapies for the treatment of cancer and other diseases, today announced its financial results for the quarter ended June 30, 2026, and provided a corporate update highlighting clinical progress for Plinabulin and the Company’s leadership transition.

“The second quarter was marked by additional clinical and scientific support for continuing Plinabulin development,” said Min Qiu, Chief Executive Officer of BeyondSpring. “Updated Phase 2 data presented at ASCO 2026 continued to demonstrate an encouraging 58% two-year OS rate in metastatic NSCLC patients whose disease progressed after first-line immune checkpoint inhibitor (ICI) therapy. This encouraging prospective OS data strengthens our conviction in the DUBLIN-4 study, a confirmatory Phase 3 study with OS as the primary endpoint in non-squamous NSCLC post-ICI with no driver mutation, a severe unmet medical need with docetaxel as the standard of care. With our leadership transition now effective, our priorities are clear: advancing the regulatory, operational and financing preparations necessary to initiate DUBLIN-4.”

Mr. Qiu continued, “The DUBLIN-4 study represents our lead clinical development priority for a potential path toward future regulatory submissions. We believe the published DUBLIN-3 results in The Lancet Respiratory Medicine, recent ASCO 2026 clinical data, and the AACR 2026 ADC combination findings collectively reinforce Plinabulin’s differentiated potential as a potent dendritic cell maturation agent to improve survival benefits while mitigating treatment-limiting high-grade neutropenia in NSCLC and beyond.”

Recent Clinical and Corporate Highlights of Plinabulin

ASCO 2026 (Phase 2 data): Plinabulin combination demonstrated durable response and survival benefit in post-ICI metastatic NSCLC

  • Presented updated efficacy and safety results from the investigator-initiated Phase 2 303 Study evaluating Plinabulin/docetaxel and pembrolizumab in 47 patients with metastatic NSCLC and acquired resistance following first-line immune checkpoint inhibitor therapy.
  • As of the February 28, 2026 data cutoff, median progression-free survival was 7.0 months, median duration of response was 9.3 months, disease control rate was 79.5%, and confirmed objective response rate was 18.2%.
  • The 12-month and 24-month overall survival rates were 78.1% and 58.0%, respectively, with median overall survival not reached after a median follow-up of 28.8 months.
  • The combination demonstrated a generally manageable safety profile and evidence of immune activation, including increased frequencies of activated CD4+ and CD8+ T cells as well as higher white blood cell, neutrophil, and platelet counts.

AACR 2026 (preclinical data): Improved complete response rate, overall survival and tolerability of certain antibody-drug-conjugates (ADCs)

  • Presented preclinical data showing that Plinabulin in combination with the approved topoisomerase I inhibitor (TOP1)-based ADCs enhanced complete tumor regression rates and/or survival of TROP-2-directed datopotamab deruxtecan or HER2-directed trastuzumab deruxtecan, with or without PD-1/PD-L1 inhibition.
  • Plinabulin improved tolerability in the preclinical combination models and increased the CD8+ T-cell-to-Treg ratio, supporting an immune-mediated mechanism for the enhanced anticancer activity.
  • The findings support Plinabulin’s potential to address limited durability and treatment-limiting hematologic toxicity associated with ADC-based therapy and broaden the scientific rationale for future ADC combination studies.

DUBLIN-4 Confirmatory Phase 3 Program

  • DUBLIN-4 is the Company’s planned, randomized, double-blind, 442-patient confirmatory Phase 3 study of Plinabulin plus docetaxel in non-squamous, EGFR wild-type NSCLC patients who have progressed on PD-1/PD-L1 inhibitor-containing therapies.
  • The program is designed to prospectively confirm the survival and tolerability benefits observed in the DUBLIN-3 Phase 3 study, which was published in The Lancet Respiratory Medicine in 2024.

BeyondSpring Leadership Transition and Corporate Execution

  • Effective July 1, 2026, Min Qiu was appointed Chief Executive Officer with a mandate focused on advancing DUBLIN-4, extending Plinabulin’s scientific optionality, and building BeyondSpring’s global partner and investor base. Dr. Jiangwen (Jen) Majeti was appointed Vice Chairman, strengthening Board-level governance continuity and strategic depth. Na Li was appointed Chief Financial Officer to support financial discipline, public-company reporting, financing activities, and capital markets engagement.
  • Dr. Lan Huang remains Co-Founder and Chairman of BeyondSpring, providing strategic vision and Board leadership, while devoting her executive focus to SEED Therapeutics, where she serves as Co-Founder, Chairman, and Chief Executive Officer.

Second Quarter Financial Results

Continuing operations:

  • Research and development (R&D) expenses were $1.0 million for the quarter ended June 30, 2026, compared to $1.0 million for the quarter ended June 30, 2025. R&D expenses remained relatively flat, as a $0.3 million increase in drug manufacturing activities to prepare for potential future study initiation was substantially offset by lower patent-related professional services and personnel expenses.
  • General and administrative (G&A) expenses were $0.8 million for the quarter ended June 30, 2026, compared to $0.9 million for the quarter ended June 30, 2025. The $0.1 million decrease was primarily due to lower legal and consulting expenses related to accounting advisory and business development.
  • Net loss was $1.8 million for the quarter ended June 30, 2026, compared to $1.9 million for the quarter ended June 30, 2025.
  • Cash, cash equivalents, and short-term investments were $6.5 million as of June 30, 2026, compared to $12.6 million as of December 31, 2025.

Year-to-Date Financial Results

Continuing operations:

  • Research and development (R&D) expenses were $2.0 million for the six months ended June 30, 2026, compared to $1.9 million for the six months ended June 30, 2025. The $0.1 million increase was primarily due to higher drug manufacturing expenses, partially offset by lower patent-related professional services, regulatory filing advisory and personnel expenses.
  • General and administrative (G&A) expenses were $1.9 million for the six months ended June 30, 2026, compared to $2.7 million for the six months ended June 30, 2025. The $0.8 million decrease was primarily due to lower incentive compensation and share-based compensation and lower professional services expenses related to legal advisory matters.
  • Net loss was $4.1 million for the six months ended June 30, 2026, compared to $4.5 million for the six months ended June 30, 2025.

About BeyondSpring

BeyondSpring (NASDAQ: BYSI) is a clinical-stage biopharmaceutical company developing first-in-class therapies for cancers with high unmet needs. Its lead asset, Plinabulin, has been studied in over 700 cancer patients and is in late-stage development across multiple cancer indications, with results published in The Lancet Respiratory Medicine. Plinabulin’s novel mechanism as a GEF-H1 agonist with dendritic cell maturation benefit supports both anticancer activity and immune modulation, offering a unique approach to re-sensitizing tumors resistant to checkpoint inhibitors. In addition, it has the potential to synergize with chemotherapy, antibody-drug conjugates (ADCs), radiation, and checkpoint inhibitors. Learn more at beyondspringpharma.com.

Investor Contact: IR@beyondspringpharma.com
Media Contact: PR@beyondspringpharma.com

Cautionary Note Regarding Forward-Looking Statements

This press release includes forward-looking statements that are not historical facts. Words such as “will,” “expect,” “anticipate,” “plan,” “believe,” “design,” “may,” “future,” “estimate,” “predict,” “objective,” “goal,” or variations thereof and similar expressions are intended to identify such forward-looking statements. Forward-looking statements are based on BeyondSpring’s current knowledge, beliefs, and expectations regarding possible future events and are subject to risks, uncertainties, and assumptions. Actual results and the timing of events could differ materially from those anticipated in these forward-looking statements as a result of a number of factors, including, but not limited to, difficulties raising the anticipated amount needed to finance the Company’s future operations on terms acceptable to the Company, if at all; unexpected results from preclinical studies or clinical trials; the risk that preclinical results may not be predictive of clinical results; delays in, or failure to obtain, regulatory approvals; results that do not meet the Company’s expectations regarding the safety, efficacy, clinical utility, or regulatory pathway of the Company’s product candidates; increased competition in the market; the Company’s ability to meet Nasdaq’s continued listing requirements; and other risks described in BeyondSpring’s most recent Form 10-K and subsequent filings with the U.S. Securities and Exchange Commission. All forward-looking statements made herein speak only as of the date of this release, and BeyondSpring undertakes no obligation to update publicly such forward-looking statements to reflect subsequent events or circumstances, except as otherwise required by law.

Financial Tables to Follow

    
BEYONDSPRING INC.

CONDENSED CONSOLIDATED BALANCE SHEETS

(Amounts in thousands of U.S. Dollars ($), except for number of shares and per share data)
    
  As of
  December 31,
2025
  June 30,
2026
 
   $   $ 
      (Unaudited) 
Assets        
Current assets:        
Cash and cash equivalents  7,786   2,697 
Short-term investments  4,775   3,832 
Advances to suppliers  227   247 
Prepaid expenses and other current assets  71   273 
Current assets of discontinued operations  8,023   2,852 
Total current assets  20,882   9,901 
         
Noncurrent assets:        
Property and equipment, net  166   138 
Operating right-of-use assets  305   174 
Other noncurrent assets  224   128 
Noncurrent assets of discontinued operations  4,356   4,265 
Total noncurrent assets  5,051   4,705 
         
Total assets  25,933   14,606 
         
Liabilities and equity        
         
Current liabilities:        
Accounts payable  363   790 
Accrued expenses  938   1,390 
Current portion of operating lease liabilities  320   171 
Other current liabilities  822   1,055 
Current liabilities of discontinued operations  11,133   10,787 
Total current liabilities  13,576   14,193 
         
Noncurrent liabilities:        
Deferred revenue  28,600   29,476 
Other noncurrent liabilities  3,981   4,420 
Noncurrent liabilities of discontinued operations  3,766   2,542 
Total noncurrent liabilities  36,347   36,438 
         
Total liabilities  49,923   50,631 
         
         
         
Shareholdersdeficit        
Ordinary shares ($0.0001 par value; 500,000,000 shares authorized; 41,122,320 and 41,119,820 shares issued and outstanding as of December 31, 2025 and June 30, 2026, respectively)  4   4 
Additional paid-in capital  375,664   375,814 
Accumulated deficit  (408,431)  (411,439)
Accumulated other comprehensive income  602   55 
         
Total BeyondSpring Inc.’s shareholders’ deficit  (32,161)  (35,566)
Noncontrolling interests  8,171   (459)
Total shareholders’ deficit  (23,990)  (36,025)
         
Total liabilities and shareholdersdeficit  25,933   14,606 
         


BEYONDSPRING INC.

CONDENSED CONSOLIDATED STATEMENTS OF COMPREHENSIVE INCOME (LOSS)

(Amounts in thousands of U.S. Dollars ($), except for number of shares and per share data)

(Unaudited)
       
  Three months ended June 30, Six months ended June 30,
  2025  2026  2025  2026 
  $  $  $  $ 
                 
Revenue  -   -   -   - 
                 
Operating expenses                
Research and development  (1,002)  (973)  (1,876)  (2,049)
General and administrative  (947)  (758)  (2,683)  (1,914)
                 
Loss from operations  (1,949)  (1,731)  (4,559)  (3,963)
Foreign exchange gain, net  47   61   76   111 
Interest income  28   4   45   12 
Other income, net  18   16   18   31 
                 
Loss before income tax  (1,856)  (1,650)  (4,420)  (3,809)
Income tax expenses  (22)  (100)  (42)  (292)
                 
Net loss from continuing operations  (1,878)  (1,750)  (4,462)  (4,101)
                 
Discontinued operations                
Loss from discontinued operations  (2,771)  (3,950)  (6,003)  (8,273)
Gain on sale of subsidiary interests  -   -   6,986   - 
Income tax expenses  -   -   -   - 
Net income (loss) from discontinued operations  (2,771)  (3,950)  983   (8,273)
                 
Net loss  (4,649)  (5,700)  (3,479)  (12,374)
Less: Net loss attributable to noncontrolling interests from continuing operations  (72)  (841)  (147)  (973)
Less: Net loss attributable to noncontrolling interests from discontinued operations  (2,771)  (4,010)  (6,003)  (8,393)
Net income (loss) attributable to BeyondSpring Inc.  (1,806)  (849)  2,671   (3,008)
                 
Earnings (loss) per share, basic and diluted                
Continuing operations  (0.04)  (0.02)  (0.11)  (0.08)
Discontinued operations  -   -   0.18   - 
Basic and diluted earnings (loss) per share  (0.04)  (0.02)  0.07   (0.08)
                 
Weighted-average shares outstanding                
Basic and diluted  40,316,320   41,119,820   40,316,320   41,119,820 
                 
Other comprehensive loss, net of tax of nil:                
Foreign currency translation adjustment loss from continuing operations  (343)  (471)  (494)  (850)
Foreign currency translation adjustment loss from discontinued operations  (27)  (70)  (34)  (117)
Comprehensive loss  (5,019)  (6,241)  (4,007)  (13,341)
Less: Comprehensive loss attributable to noncontrolling interests from continuing operations  (194)  (1,007)  (324)  (1,276)
Less: Comprehensive loss attributable to noncontrolling interests from discontinued operations  (2,798)  (4,080)  (6,037)  (8,510)
Comprehensive income (loss) attributable to BeyondSpring Inc.  (2,027)  (1,154)  2,354   (3,555)
                 



FAQ

How did BeyondSpring (NASDAQ: BYSI) perform financially in Q2 2026?

BeyondSpring reported a Q2 2026 net loss from continuing operations of $1.8 million and no revenue. According to BeyondSpring, R&D expenses were $1.0 million, G&A expenses were $0.8 million, and cash, cash equivalents and short-term investments totaled $6.5 million at quarter‑end.

What were the key ASCO 2026 results for Plinabulin in metastatic NSCLC post-ICI?

The ASCO 2026 Phase 2 study showed a 58.0% 24‑month overall survival rate in metastatic NSCLC patients post‑ICI. According to BeyondSpring, median progression‑free survival was 7.0 months, median duration of response 9.3 months, disease control rate 79.5%, and the safety profile was generally manageable.

What is the design of BeyondSpring’s planned DUBLIN-4 Phase 3 trial in NSCLC?

DUBLIN‑4 is a planned randomized, double‑blind, 442‑patient confirmatory Phase 3 trial of Plinabulin plus docetaxel. According to BeyondSpring, it will enroll non‑squamous, EGFR wild‑type NSCLC patients who have progressed on PD‑1/PD‑L1 therapies, aiming to prospectively confirm survival and tolerability seen in DUBLIN‑3.

What did AACR 2026 preclinical data show about Plinabulin in ADC combinations?

AACR 2026 preclinical data showed Plinabulin enhanced complete tumor regression, survival and tolerability with certain TOP1‑based ADCs. According to BeyondSpring, combinations with TROP‑2‑directed and HER2‑directed ADCs improved outcomes and increased CD8+ T‑cell‑to‑Treg ratios, supporting an immune‑mediated mechanism and future ADC combination studies.

How has BeyondSpring’s cash position and balance sheet changed by June 30, 2026?

BeyondSpring held $6.5 million in cash, cash equivalents and short‑term investments at June 30, 2026, down from $12.6 million. According to BeyondSpring, total assets were $14.6 million, total liabilities $50.6 million, resulting in a shareholders’ deficit of $36.0 million.

What leadership changes did BeyondSpring (BYSI) announce around Q2 2026?

Effective July 1, 2026, BeyondSpring appointed Min Qiu as Chief Executive Officer and Na Li as Chief Financial Officer. According to BeyondSpring, Dr. Jiangwen (Jen) Majeti became Vice Chairman, while Co‑Founder Dr. Lan Huang remains Chairman, focusing executive efforts on SEED Therapeutics.