BeyondSpring Pharmaceuticals
BeyondSpring Pharmaceuticals is a clinical-stage biopharmaceutical company developing Plinabulin, a first-in-class GEF-H1 agonist immune modulator for NSCLC patients who progress on checkpoint inhibitors, plus a minority stake in SEED Therapeutics' targeted protein degradation platform.
- Company typePublic
- Founded2014
- HeadquartersNew York, United States
- Headcount11–50
- GTM typeB2B
- OfferingHardware or Manufacturing
What BeyondSpring Pharmaceuticals does
BeyondSpring Pharmaceuticals is a clinical-stage biopharmaceutical company developing first-in-class immune-modulating cancer therapies, principally Plinabulin, a small-molecule GEF-H1 agonist that promotes dendritic cell maturation and T-cell priming. Through a unique and reversible binding to tubulin, Plinabulin is designed to restore tumor sensitivity to PD-1/PD-L1 checkpoint inhibitors while simultaneously reducing chemotherapy-induced neutropenia. The lead program targets EGFR wild-type non-squamous non-small cell lung cancer (NSCLC) patients who have progressed after immune checkpoint inhibitor therapy, an indication where over 60% of patients develop resistance and where nine late-stage trials have failed to improve overall survival over docetaxel. The DUBLIN-3 Phase 3 trial (n=559) demonstrated median OS of 15.8 vs 11.7 months (HR 0.55) and was published in The Lancet Respiratory Medicine in 2024; DUBLIN-4 (n=442) is being designed as the FDA-aligned confirmatory registrational study. BeyondSpring retains a minority equity stake (approximately 14.4% after the January 2025 partial sale) in SEED Therapeutics, a separately funded targeted protein degradation company co-founded with Eli Lilly in 2020 that is advancing the RITE3 molecular glue platform with its lead RBM39 degrader ST-01156 entering Phase 1.
BeyondSpring operates as a pre-revenue clinical-stage company with no current product sales, generating no revenue and reporting a Q1 2026 net loss of $2.4 million from continuing operations. The business model is oriented toward eventual commercialization of Plinabulin through standard pharmaceutical channels (wholesale distributors, specialty pharmacies, hospital purchasing) following regulatory approval, with go-to-market planned via direct engagement with oncologists, key opinion leaders, and academic medical centers. Current revenue-equivalents derive from monetizing a portion of the SEED Therapeutics equity stake ($35.4 million sold in January 2025). Clinical development is supported by investigator-initiated studies at top cancer centers (MD Anderson, Memorial Sloan Kettering, Peking Union Medical College Hospital, Wuhan Union Hospital, Shanghai Chest Hospital) and through strategic drug-supply partnerships, notably with Merck (pembrolizumab supply for Studies 303 and 302). The company holds composition-of-matter patent protection for Plinabulin through 2036 in 40+ jurisdictions, with Hatch-Waxman extension potentially extending exclusivity to 2041.
BeyondSpring Pharmaceuticals firmographics
Firmographics- Name
- BeyondSpring Pharmaceuticals
- Legal name
- BeyondSpring Inc.
- Website
- https://beyondspringpharma.com
- Company type
- Public
- Founded year
- 2014
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Short description
- BeyondSpring Pharmaceuticals is a clinical-stage biopharmaceutical company developing Plinabulin, a first-in-class GEF-H1 agonist immune modulator for NSCLC patients who progress on checkpoint inhibitors, plus a minority stake in SEED Therapeutics' targeted protein degradation platform.
- Ownership category
- akta.pro rank
BeyondSpring Pharmaceuticals industry classification
Industry- Product category
- Oncology Pharmaceuticals
- NAICS
- Pharmaceutical and Medicine Manufacturing (3254), Research and Development in Biotechnology (except Nanobiotechnology) (541714)
- SIC
- Pharmaceutical Preparations (2834)
- akta.pro primary industry
- Primary Care & General Medicine Pharmaceuticals (HLAIAAAA)
- akta.pro secondary industries
- Small-Molecule CMC Documentation & Regulatory Support (DMF/CMC) (HLAGAHAM), GMP Scale-Up, Tech Transfer & Process Validation (PPQ) (HLAGAHAL)
Keywords
Where BeyondSpring Pharmaceuticals is headquartered
LocationHeadquarters
- HQ city
- New York
- HQ country
- United States
- HQ region
- North America
Offices1 record
Markets served
BeyondSpring Pharmaceuticals business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Technology or R&D, Personnel, Operations, Marketing or Sales
Revenue model
- Future Product Sales: BeyondSpring is a clinical-stage biopharmaceutical company with no current revenue. The company is developing Plinabulin for cancer treatment and expects to generate revenue through product sales following regulatory approval. The company also retains equity stake in SEED Therapeutics (~14-38% ownership) which may generate future value.
Go-to-market motion1 record
Distribution channels1 record
Marketing channels6 records
BeyondSpring Pharmaceuticals product offering
Product offeringCore offering
BeyondSpring Pharmaceuticals is a clinical-stage biopharmaceutical company developing Plinabulin, a first-in-class GEF-H1 agonist that promotes dendritic cell maturation for cancer treatment, with lead indications in non-small cell lung cancer (NSCLC) patients who have progressed after PD-1/PD-L1 checkpoint inhibitor therapy. The company also operates SEED Therapeutics, a subsidiary developing targeted protein degradation therapeutics using the proprietary RITE3 molecular glue platform, with lead candidate ST-01156 (RBM39 degrader) entering Phase 1 clinical development.
Product overview
BeyondSpring Pharmaceuticals is a clinical-stage biopharmaceutical company developing first-in-class immune-modulating cancer therapies. The company's lead product is Plinabulin, a GEF-H1 agonist and first-in-class dendritic cell maturation agent that has been studied in over 700 cancer patients across multiple Phase 1-3 clinical trials. Plinabulin is in late-stage development for NSCLC and other cancer indications, with positive results from the DUBLIN-3 Phase 3 trial published in The Lancet Respiratory Medicine. The company is advancing DUBLIN-4, a confirmatory Phase 3 registrational trial. The portfolio also includes SEED Therapeutics, a subsidiary developing targeted protein degradation therapeutics using the proprietary RITE3 molecular glue platform, with ST-01156 (RBM39 degrader) entering Phase 1 clinical development.
Differentiator
Problem solved
Functional benefit
Products and services
- Plinabulin First-in-class, small-molecule immune modulator (GEF-H1 agonist) with differentiated mechanism for cancer treatment. Promotes dendritic cell maturation and robust T-cell priming, driving anti-tumor immune response. Studied in over 700 cancer patients across multiple Phase 1-3 clinical trials. Indicated for NSCLC patients who have progressed after PD-1/PD-L1 checkpoint inhibitor therapy.
Quantifiable outcome
- Median OS improvement: 15.8 vs 11.7 months (HR=0.55) in non-squamous EGFR WT NSCLC post anti-PD-(L)1
- +5 more outcomes
Companies that use BeyondSpring Pharmaceuticals
Customer profileNamed customers5 records
Segments3 records
Ideal customer profiles1 record
BeyondSpring Pharmaceuticals technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature5 records
BeyondSpring Pharmaceuticals partnerships and signals
Strategic signalPartnerships
Eight partnerships are on record, tiered core.
- SEED Therapeutics Inc.coreSEED Therapeutics is a clinical-stage biotechnology company co-founded by BeyondSpring focused on targeted protein degradation. BeyondSpring retains approximately 14-38% equity stake following Series A-3 financing. SEED advances its RITE3 platform with lead program ST-01156 (RBM39 degrader) in Phase 1 clinical development.
- Wuhan Union HospitalcorePhase 2 investigator-initiated study (NCT05745350) at Wuhan Union Hospital evaluating pembrolizumab, Plinabulin plus etoposide/platinum as first-line therapy for extensive-stage small cell lung cancer (ES-SCLC), with Dr. Xiaorong Dong as principal investigator.
- Merck (MSD) - Investigator Studies ProgramcoreMerck provides funding and study drug (pembrolizumab/Keytruda) for investigator-initiated studies including Study 303 in NSCLC (NCT05599789) and Study 302 in SCLC (NCT05745350). Studies evaluate Plinabulin's ability to resensitize tumors to PD-1 checkpoint inhibitors through dendritic cell maturation.
- Eli Lilly and CompanycoreBeyondSpring co-founded SEED Therapeutics with Eli Lilly in 2020. Lilly is a cornerstone investor and collaborator in targeted protein degradation research. SEED's Series A-3 financing was led by Eisai with continued involvement from Lilly. Collaboration focuses on developing molecular glue degraders using SEED's RITE3 platform for diseases driven by undruggable proteins.
- Peking Union Medical College HospitalcorePhase 2 investigator-initiated Study 303 conducted at Peking Union Medical College Hospital in Beijing, China, evaluating Plinabulin plus docetaxel and pembrolizumab in 47 metastatic NSCLC patients who progressed on prior PD-1/L1 inhibitors.
- MD Anderson Cancer CentercorePhase 1 investigator-initiated study (NCT04902040) at MD Anderson demonstrating Plinabulin's ability to promote DC maturation and M1 macrophage polarization via GEF-H1-dependent mechanism in patients with 8 cancer types who failed prior PD-1/L1 inhibitors.
- Memorial Sloan Kettering Cancer CentercorePhase 1 investigator-initiated study collaboration in multiple myeloma patients undergoing autologous hematopoietic stem cell transplantation (AHCT), evaluating Plinabulin's ability to reduce infectious neutropenic fever and transfusion requirements.
- Shanghai Chest HospitalcoreCollaboration with Shanghai Chest Hospital for ADC combination preclinical and clinical development, demonstrating China's ADC research ecosystem value in advancing Plinabulin's global development.
Scale indicators10 records
Recent moves7 records
Expansion highlights5 records
BeyondSpring Pharmaceuticals competitors and assessment
Company assessmentDirect peers
- Arcus Biosciences: Clinical-stage immuno-oncology company developing combinations with checkpoint inhibitors (including adenosine and TIGIT pathways). Most directly comparable to BeyondSpring for its I/O-combination development strategy in NSCLC and other tumor types.
- Compugen: Clinical-stage immuno-oncology company focused on novel drug targets that combine with PD-1 inhibitors to overcome resistance. Comparable therapeutic thesis to Plinabulin's dendritic cell maturation approach for checkpoint-resistant tumors.
- Erasca: Clinical-stage precision oncology company developing therapies targeting the RAS/MAPK pathway with combination strategies. Similar clinical-stage profile and oncology development focus; also notable as BeyondSpring board member Jen Majeti previously served as Erasca's Head of Global Collaborations.
- Cogent Biosciences: Clinical-stage precision oncology company developing small-molecule kinase inhibitors for genomically defined cancers. Similar small-molecule clinical-stage profile with comparable capitalization and oncology focus.
- Spectrum Pharmaceuticals: Commercial and clinical-stage oncology company with a portfolio of hematology and oncology drugs including lung cancer products. Comparable oncology commercial-readiness profile though broader portfolio.
- Black Diamond Therapeutics: Clinical-stage precision oncology company developing small-molecule therapies against allosteric oncogenic mutations. Similar clinical-stage profile and small-molecule oncology development approach.
- Checkpoint Therapeutics: Clinical-stage immuno-oncology company developing anti-PD-L1 antibodies and targeted small molecules for lung cancer and other tumors. Direct overlap in checkpoint inhibitor + combination strategy for NSCLC.
Emerging players
- Mirati Therapeutics: Pre-acquisition by Bristol-Myers Squibb, Mirati was a clinical-stage oncology company focused on targeted oncology (KRAS, PRMT5) for NSCLC. Direct peer in lung cancer drug development though now part of BMS.
- Turning Point Therapeutics: Pre-acquisition by BMS, Turning Point was a clinical-stage precision oncology company developing next-gen kinase inhibitors for NSCLC. Comparable lung cancer drug development focus though now under BMS ownership.
Broad incumbents
- Blueprint Medicines: Commercial-stage precision therapy company developing kinase-targeted small molecules for oncology and rare diseases. Comparable small-molecule oncology drug developer with broader portfolio than BeyondSpring's single-asset focus.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat4 records
Key risks7 records
Key highlights7 records
Customer concentration
BeyondSpring Pharmaceuticals social profiles
Digital presenceBeyondSpring Pharmaceuticals financial estimates
Financial estimateRevenue estimate
Valuation estimate
BeyondSpring Pharmaceuticals leadership team
Management profileNumber of profiles
Profiles10 records
BeyondSpring Pharmaceuticals subsidiaries and ownership
Company hierarchySubsidiaries2 records
BeyondSpring Pharmaceuticals funding detail
Funding detailFunding overview
Funding rounds3 records
Investors3 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
BeyondSpring Pharmaceuticals M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about BeyondSpring Pharmaceuticals
What does BeyondSpring Pharmaceuticals do?
BeyondSpring Pharmaceuticals is a clinical-stage biopharmaceutical company developing Plinabulin, a first-in-class GEF-H1 agonist that promotes dendritic cell maturation for cancer treatment, with lead indications in non-small cell lung cancer (NSCLC) patients who have progressed after PD-1/PD-L1 checkpoint inhibitor therapy. The company also operates SEED Therapeutics, a subsidiary developing targeted protein degradation therapeutics using the proprietary RITE3 molecular glue platform, with lead candidate ST-01156 (RBM39 degrader) entering Phase 1 clinical development.
Is BeyondSpring Pharmaceuticals a public or private company?
BeyondSpring Pharmaceuticals is a public company. It is classified as public and is currently operating.
When was BeyondSpring Pharmaceuticals founded?
BeyondSpring Pharmaceuticals was founded in 2014. It employs 11 to 50 people.
Where is BeyondSpring Pharmaceuticals based?
BeyondSpring Pharmaceuticals is headquartered in New York, United States, in the North America region.
How does BeyondSpring Pharmaceuticals make money?
One revenue line is on record: future Product Sales.
Who are BeyondSpring Pharmaceuticals's main competitors?
Direct peers on record are Arcus Biosciences, Compugen, Erasca, Cogent Biosciences, Spectrum Pharmaceuticals, Black Diamond Therapeutics and Checkpoint Therapeutics. Emerging players are Mirati Therapeutics and Turning Point Therapeutics. Blueprint Medicines is listed as a broad incumbent.
Does BeyondSpring Pharmaceuticals have an API?
No public API is recorded for BeyondSpring Pharmaceuticals.
What industry is BeyondSpring Pharmaceuticals in?
BeyondSpring Pharmaceuticals's product category is Oncology Pharmaceuticals. Its primary akta.pro industry code is HLAIAAAA, Primary Care & General Medicine Pharmaceuticals, with a secondary code of HLAGAHAM, Small-Molecule CMC Documentation & Regulatory Support (DMF/CMC). Its NAICS code is 3254 and its SIC code is 2834.