STOCK TITAN

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

Rhea-AI Impact
(High)
Rhea-AI Sentiment
(Neutral)
Tags

BeyondSpring (NASDAQ:BYSI) reported Q1 2026 results and pipeline updates. Continuing operations showed R&D and G&A expenses of $1.1M each, net loss of $2.4M, and $7.9M in cash and investments.

Plinabulin preclinical data supported its use with ADCs, while SEED’s ST-01156 entered Phase 1 with biomarker-driven development.

Loading...
Loading translation...

AI-generated analysis. Not financial advice.

Positive

  • Plinabulin preclinical ADC combinations improved response, survival, tolerability, and CD8+/Treg ratio
  • ST-01156 RBM39 molecular glue advanced into Phase 1; first dose cohort completed
  • AACR 2026 data showed complete tumor eradication in a neuroblastoma in vivo model
  • G&A expenses from continuing operations fell to $1.1M from $1.7M year over year
  • Net loss from continuing operations narrowed to $2.4M from $2.6M year over year

Negative

  • Net loss from continuing operations was $2.4M in Q1 2026
  • Discontinued operations recorded a $4.3M net loss versus $3.8M net income a year earlier
  • R&D expenses from continuing operations increased to $1.1M from $0.9M year over year

News Market Reaction – BYSI

+4.32%
3 alerts
+4.32% News Effect
+5.2% Peak Tracked
+$3M Valuation Impact
$66.61M Market Cap
0.5x Rel. Volume

On the day this news was published, BYSI gained 4.32%, reflecting a moderate positive market reaction. Argus tracked a peak move of +5.2% during that session. Our momentum scanner triggered 3 alerts that day, indicating moderate trading interest and price volatility. This price movement added approximately $3M to the company's valuation, bringing the market cap to $66.61M at that time.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

R&D expenses: $1.1M R&D expenses prior-year: $0.9M G&A expenses: $1.1M +5 more
8 metrics
R&D expenses $1.1M Three months ended March 31, 2026 (continuing operations)
R&D expenses prior-year $0.9M Three months ended March 31, 2025 (continuing operations)
G&A expenses $1.1M Three months ended March 31, 2026 (continuing operations)
G&A expenses prior-year $1.7M Three months ended March 31, 2025 (continuing operations)
Net loss continuing ops $2.4M Three months ended March 31, 2026
Net loss continuing prior-year $2.6M Three months ended March 31, 2025
Cash & equivalents $7.9M As of March 31, 2026
Discontinued ops net loss $4.3M Three months ended March 31, 2026 (vs. $3.8M net income in 2025)

Market Reality Check

Price: $1.5000 Vol: Volume 5,447 is below the...
low vol
$1.5000 Last Close
Volume Volume 5,447 is below the 20-day average of 9,953 (relative volume 0.55x). low
Technical Shares at $1.39 are trading below the $1.75 200-day moving average and well under the $3.44 52-week high.

Peers on Argus

BYSI is down 8.55% while key biotech peers show mixed moves: IMMX up 6.81%, ALGS...
1 Up

BYSI is down 8.55% while key biotech peers show mixed moves: IMMX up 6.81%, ALGS up 4.19%, OSTX down 1.72%, ACET down 2.69%, IGMS down 2.31%. Combined with scanner data showing only OSTX in momentum, the pattern points to a stock-specific reaction.

Previous Earnings Reports

4 past events · Latest: Mar 25 (Positive)
Same Type Pattern 4 events
Date Event Sentiment Move Catalyst
Mar 25 Year-end earnings Positive +3.7% 2025 year-end results with Phase 3 success and SEED progress highlighted.
Nov 12 Q3 2025 earnings Positive -3.6% Q3 2025 data showing strong NSCLC metrics and SEED financing progress.
Aug 13 Q2 2025 earnings Positive -0.5% Q2 2025 update with promising Plinabulin data and SEED IND clearance.
May 12 Q1 2025 earnings Positive +4.3% Q1 2025 results plus early clinical success and SEED pipeline advances.
Pattern Detected

Earnings-related releases have produced mixed reactions, with two positive and two negative 24-hour moves despite generally constructive clinical and financial updates.

Recent Company History

Over the past year, BeyondSpring’s earnings updates have consistently paired oncology progress with evolving financials. The Q2 2025 and Q3 2025 results highlighted Plinabulin’s activity in NSCLC and multiple cancer types, plus SEED’s RBM39 degrader advances and financings. The 2025 year-end release emphasized positive Phase 3 DUBLIN-3 data, plans for DUBLIN-4, and cash of $12.6M as of Dec 31, 2025. Today’s Q1 2026 update continues this pattern, showing modestly lower net loss and focused R&D and G&A spending alongside pipeline momentum.

Historical Comparison

+0.9% avg move · In the past four earnings releases, BYSI’s average 24-hour move was 0.95%, with reactions split betw...
earnings
+0.9%
Average Historical Move earnings

In the past four earnings releases, BYSI’s average 24-hour move was 0.95%, with reactions split between gains and losses. Today’s sharper -8.55% drop stands out versus that history.

Earnings updates trace Plinabulin’s evolution from Phase 1–2 signals to Phase 3 DUBLIN-3 success and a planned DUBLIN-4 trial, while SEED’s RBM39 degrader advanced from IND clearance into Phase 1 and attracted Series A-3 financing.

Market Pulse Summary

This announcement combines Q1 2026 financial results with pipeline updates for Plinabulin and SEED’s...
Analysis

This announcement combines Q1 2026 financial results with pipeline updates for Plinabulin and SEED’s RBM39 degrader ST‑01156. BeyondSpring reported R&D and G&A expenses of $1.1M each, a net loss from continuing operations of $2.4M, cash of $7.9M, and a $4.3M loss from discontinued operations. Historically, earnings updates have intertwined clinical milestones and funding needs, so investors may watch burn trends, SEED’s discontinued-operations performance, and progress into Phase 3 and Phase 1 trials as key future catalysts.

Key Terms

antibody-drug conjugate (ADC), molecular glue degrader, biomarker-driven, immune checkpoint inhibitors, +4 more
8 terms
antibody-drug conjugate (ADC) medical
"Plinabulin as a Potential Backbone Agent to Combine with Antibody-Drug Conjugate (ADC)-Based Therapies"
An antibody-drug conjugate (ADC) is a targeted medical treatment that combines an antibody, which acts like a guided missile seeking out specific cells, with a powerful drug to destroy those cells. It is designed to deliver medication directly to diseased cells, minimizing damage to healthy tissue. For investors, ADCs represent innovative therapies with potential for high growth, especially if they prove effective in treating difficult-to-cure conditions.
molecular glue degrader medical
"SEED Advances First Molecular Glue Degrader into Clinical Development"
A molecular glue degrader is a small drug-like molecule that acts like a tiny adhesive, sticking a specific disease-related protein to the cell’s natural disposal machinery so the protein is destroyed rather than merely blocked. Investors watch these compounds because they can turn previously untreatable targets into removable liabilities, potentially creating breakthrough therapies, shifting development risk, and offering strong commercial upside if clinical results and regulatory approval follow.
biomarker-driven medical
"into clinical development in oncology indications, coupled with a biomarker-driven approach"
An approach where medical decisions—like choosing patients for a treatment or designing a clinical trial—are guided by measurable biological signs (such as a gene change, protein level, or imaging result). For investors, biomarker-driven programs can raise the odds of clinical success, shrink development costs and speed regulatory review by targeting therapies to the people most likely to benefit, much like using a map to find the best route instead of driving aimlessly.
immune checkpoint inhibitors medical
"ADC regimens, with or without immune checkpoint inhibitors"
Drugs that release the immune system’s natural “brakes,” allowing immune cells to recognize and attack cancer cells; imagine taking the safety off a guard dog so it can chase intruders. They matter to investors because they can become high-value treatments with large sales potential, but their commercial success depends on clinical trial results, regulatory approval, competition and side-effect management, which all affect a company’s valuation.
CD8+ T cell / Treg ratio medical
"Enhanced CD8+ T cell / Treg ratio - shifting the tumor immune environment"
The CD8+ T cell / Treg ratio compares the number of killer immune cells (CD8+ T cells that attack infected or cancerous cells) to suppressor immune cells (regulatory T cells, or Tregs, that calm immune responses). Investors care because this balance is a simple biomarker of how strongly the immune system is fighting a disease or responding to a therapy—like measuring the number of firefighters versus traffic controllers at a blaze—which can influence drug efficacy, trial success, and commercial prospects.
Phase 1 clinical development medical
"ST-01156 ... advanced into Phase 1 clinical development, with the first dose cohort completed"
Phase 1 clinical development is the first stage of testing a new drug or medical treatment in people, typically involving a small group to check safety, how the body processes the treatment, and to identify common side effects. For investors, it matters because successful Phase 1 results reduce early risk, validate basic safety and dosing, and create the first clinical evidence that a program can advance—key milestones that influence funding, valuation and future trial timelines.
discontinued operations financial
"SEED’s operations met the criteria as discontinued operations under ASC 205-20"
Discontinued operations are parts of a company that it has decided to sell or shut down, and no longer plans to run in the future. This matters to investors because it helps them understand which parts of the business are ongoing and which are being phased out, providing a clearer picture of the company’s current performance and future prospects. Think of it like a store closing a department—it no longer contributes to sales or profits.
ASC 205-20 regulatory
"met the criteria as discontinued operations under ASC 205-20 for financial reporting purposes"
A U.S. accounting standard that sets the rules for when a company must report a major part of its business as a "discontinued operation" and how to show the related results on financial statements. It matters to investors because labeling a business as discontinued separates past performance and any one-time gains or losses from ongoing operations, much like pulling a movie clip out of a long film so viewers can judge the remaining story more clearly, improving comparability and decision-making.

AI-generated analysis. Not financial advice.

AACR 2026 Data Positions Plinabulin as a Potential Backbone Agent to Combine with Antibody-Drug Conjugate (ADC)-Based Therapies to Improve Anti-Cancer Efficacy and Tolerability

SEED Advances First Molecular Glue Degrader into Clinical Development with Biomarker-Driven Strategy

FLORHAM PARK, N.J., May 13, 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 March 31, 2026, and provided a corporate update highlighting significant scientific and clinical advancements across its pipeline.

“Plinabulin continues to demonstrate the ability to enhance both efficacy and tolerability in ADC-based regimens, supporting its positioning as a potential backbone agent across a rapidly evolving treatment landscape,” said Dr. Lan Huang, Co-Founder, Chair, and Chief Executive Officer of BeyondSpring. “Data presented at AACR 2026 further highlights the expanding value of our pipeline and reinforces our strategy of advancing highly differentiated therapies with the potential to address significant unmet medical needs. We believe Plinabulin has the potential to become a foundational combination agent that unlocks the full clinical and commercial value of ADC therapies.”

Dr. Huang continued, “At SEED, the advancement of ST-01156, a novel RBM39 molecular glue degrader, into clinical development in oncology indications, coupled with a biomarker-driven approach, underscores the strength and scalability of our RITE3™ platform. These milestones reflect disciplined execution across our portfolio and position us to unlock meaningful long-term value through multiple clinical and strategic partnership opportunities.”

Recent Clinical Highlights

Plinabulin: Expanding Role as a Potentially Foundational Combination Therapy

  • AACR 2026 data demonstrated that Plinabulin significantly enhances both efficacy and tolerability of topoisomerase inhibitor–based ADC regimens, with or without immune checkpoint inhibitors
  • Preclinical findings showed:
    • Improved complete response rate and survival outcomes
    • Improved tolerability
    • Enhanced CD8+ T cell / Treg ratio - shifting the tumor immune environment from suppression to attack
  • These preclinical results suggest Plinabulin’s potential to address key limitations of current ADC therapies, including limited durability and dose-limiting safety concerns, and support Plinabulin’s positioning as a potential backbone agent across a broad range of ADC combination regimens

SEED Therapeutics: Advancing precision oncology through molecular glue degraders

  • ST-01156 (RBM39 molecular glue degrader) advanced into Phase 1 clinical development, with the first dose cohort completed
  • AACR 2026 data demonstrated:
    • Complete tumor eradication in a neuroblastoma in vivo model
    • Identification of MYC overexpression and CDKN2A/B deletion as potential predictive biomarkers
  • This program represents a biomarker-driven precision oncology approach and highlights the productivity of SEED’s proprietary RITE3™ platform for targeted protein degradation

First Quarter Financial Results1

Continuing operations:

  • R&D expenses were $1.1 million for the three months ended March 31, 2026 compared to $0.9 million for the three months ended March 31, 2025. The $0.2 million increase was primarily driven by increased drug manufacturing activities to prepare for potential future study initiation, partially offset by lower regulatory filing advisory and personnel expenses
  • G&A expenses were $1.1 million for the three months ended March 31, 2026 compared to $1.7 million for the three months ended March 31, 2025. The $0.6 million decrease was primarily driven by lower personnel and legal advisory expenses
  • Net loss was $2.4 million for the three months ended March 31, 2026 compared to $2.6 million for the three months ended March 31, 2025
  • Cash, cash equivalents, and short-term investments were $7.9 million as of March 31, 2026

Discontinued operations:

  • Net loss was $4.3 million for the three months ended March 31, 2026, compared to net income of $3.8 million for the three months ended March 31, 2025
  • Current assets were $5.3 million as of March 31, 2026

Note 1. As a result of BeyondSpring entering into definitive agreements to sell a portion of its Series A-1 Preferred Shares of SEED, SEED’s operations met the criteria as discontinued operations under ASC 205-20 for financial reporting purposes.

About BeyondSpring
BeyondSpring (NASDAQ: BYSI) is a clinical-stage biopharmaceutical company developing first-in-class therapies for cancers with high unmet need. 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. Learn more at beyondspringpharma.com.

About SEED Therapeutics
SEED Therapeutics is a clinical-stage biotechnology company pioneering targeted protein degradation. Its proprietary RITE3™ platform is advancing novel molecular glue degraders across oncology, neurodegeneration, and immunology. SEED collaborates with Eli Lilly and Company and Eisai Co., Ltd., and is advancing its RBM39 degrader into clinical development. Learn more at seedtherapeutics.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
  March 31,
2026
 
  $  $ 
      (Unaudited) 
Assets        
Current assets:        
Cash and cash equivalents  7,786   4,036 
Short-term investments  4,775   3,827 
Advances to suppliers  227   177 
Prepaid expenses and other current assets  71   181 
Current assets of discontinued operations  8,023   5,283 
Total current assets  20,882   13,504 
         
Noncurrent assets:        
Property and equipment, net  166   152 
Operating right-of-use assets  305   240 
Other noncurrent assets  224   126 
Noncurrent assets of discontinued operations  4,356   4,384 
Total noncurrent assets  5,051   4,902 
         
Total assets  25,933   18,406 
         
Liabilities and equity        
         
Current liabilities:        
Accounts payable  363   646 
Accrued expenses  938   1,278 
Current portion of operating lease liabilities  320   246 
Other current liabilities  822   937 
Current liabilities of discontinued operations  11,133   9,263 
Total current liabilities  13,576   12,370 
         
Noncurrent liabilities:        
Deferred revenue  28,600   28,994 
Other noncurrent liabilities  3,981   4,239 
Noncurrent liabilities of discontinued operations  3,766   3,157 
Total noncurrent liabilities  36,347   36,390 
         
Total liabilities  49,923   48,760 
         
         
         
Shareholders deficit        
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 March 31, 2026)  4   4 
Additional paid-in capital  375,664   375,739 
Accumulated deficit  (408,431)  (410,590)
Accumulated other comprehensive income  602   360 
         
Total BeyondSpring Inc.’s shareholders’ deficit  (32,161)  (34,487)
Noncontrolling interests  8,171   4,133 
Total shareholders’ deficit  (23,990)  (30,354)
         
Total liabilities and shareholders deficit  25,933   18,406 


 
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 March 31, 
  2025  2026 
  $  $ 
         
Revenue  -   - 
         
Operating expenses        
Research and development  (874)  (1,076)
General and administrative  (1,736)  (1,156)
         
Loss from operations  (2,610)  (2,232)
Foreign exchange gain, net  29   50 
Interest income  17   8 
Other income, net  -   15 
         
Loss before income tax  (2,564)  (2,159)
Income tax expenses  (20)  (192)
         
Net loss from continuing operations  (2,584)  (2,351)
         
Discontinued operations        
Loss from discontinued operations  (3,232)  (4,323)
Gain on sale of subsidiary interests  6,986   - 
Income tax expenses  -   - 
Net income (loss) from discontinued operations  3,754   (4,323)
         
Net income (loss)  1,170   (6,674)
Less: Net loss attributable to noncontrolling interests from continuing operations  (75)  (132)
Less: Net loss attributable to noncontrolling interests from discontinued operations  (3,232)  (4,383)
Net income (loss) attributable to BeyondSpring Inc.  4,477   (2,159)
         
Earnings (loss) per share, basic and diluted        
Continuing operations  (0.06)  (0.05)
Discontinued operations  0.17   - 
Basic and diluted earnings (loss) per share  0.11   (0.05)
         
Weighted-average shares outstanding        
Basic and diluted  40,316,320   41,119,803 
         
Other comprehensive loss, net of tax of nil:        
Foreign currency translation adjustment loss from continuing operations  (151)  (379)
Foreign currency translation adjustment loss from discontinued operations  (7)  (47)
Comprehensive income (loss)  1,012   (7,100)
Less: Comprehensive loss attributable to noncontrolling interests from continuing operations  (130)  (269)
Less: Comprehensive loss attributable to noncontrolling interests from discontinued operations  (3,238)  (4,430)
Comprehensive income (loss) attributable to BeyondSpring Inc.  4,380   (2,401)



FAQ

What were BeyondSpring (BYSI) Q1 2026 financial results from continuing operations?

BeyondSpring reported Q1 2026 continuing operations R&D and G&A expenses of $1.1M each and a net loss of $2.4M. According to BeyondSpring, this compared with $0.9M R&D, $1.7M G&A, and a $2.6M net loss in Q1 2025.

How did discontinued operations affect BeyondSpring (BYSI) Q1 2026 earnings?

Discontinued operations produced a Q1 2026 net loss of $4.3M, versus $3.8M net income a year earlier. According to BeyondSpring, SEED’s operations qualified as discontinued operations after definitive agreements to sell a portion of its Series A-1 preferred shares.

What new clinical data for Plinabulin did BeyondSpring (BYSI) highlight at AACR 2026?

AACR 2026 data showed Plinabulin enhanced efficacy and tolerability of topoisomerase inhibitor–based ADC regimens. According to BeyondSpring, preclinical results included improved complete response and survival, better tolerability, and a higher CD8+ T cell/Treg ratio, suggesting potential as a backbone ADC combination agent.

What is SEED’s ST-01156 program and its status in Q1 2026 for BeyondSpring (BYSI)?

ST-01156 is a RBM39 molecular glue degrader that entered Phase 1 oncology development, with the first dose cohort completed. According to BeyondSpring, AACR 2026 data showed complete tumor eradication in a neuroblastoma model and identified MYC overexpression and CDKN2A/B deletion as potential biomarkers.

What is BeyondSpring (BYSI) cash position as of March 31, 2026?

BeyondSpring reported cash, cash equivalents, and short-term investments of $7.9M as of March 31, 2026. According to BeyondSpring, current assets tied to discontinued operations totaled $5.3M at quarter-end, providing context for the company’s available liquidity profile.

How do BeyondSpring (BYSI) Q1 2026 R&D and G&A expenses compare year over year?

Q1 2026 R&D expenses were $1.1M, up from $0.9M, while G&A fell to $1.1M from $1.7M. According to BeyondSpring, higher R&D reflected drug manufacturing for potential studies, and lower G&A mainly reflected reduced personnel and legal advisory costs.