Skip to content
BioPharmChina BioPharmChina BioPharmChina

Covering China's BioPharma industry

BioPharmChina BioPharmChina BioPharmChina

Covering China's BioPharma industry

  • Home
  • Disease Areas
    • Oncology
    • Immunology
    • Autoimmune
    • I&I
    • Metabolic
    • Respiratory
    • Cardiovascular
    • Ophthalmology
    • Neurology
    • Rare Diseases
  • Clinical Trials
    • Phase 1
    • Phase 1/2
    • Phase 2
    • Phase 2/3
    • Phase 3
    • Phase 4
    • IIT
  • Financing
  • Manufacturing
  • Regulatory
    • FTD
    • BTD
    • IND
    • NDA/BLA
    • Approvals
  • Deals
    • M&A
    • Partnerships
  • Events
    • Conferences
    • Forums
    • Workshops
  • Companies
  • Home
  • Disease Areas
    • Oncology
    • Immunology
    • Autoimmune
    • I&I
    • Metabolic
    • Respiratory
    • Cardiovascular
    • Ophthalmology
    • Neurology
    • Rare Diseases
  • Clinical Trials
    • Phase 1
    • Phase 1/2
    • Phase 2
    • Phase 2/3
    • Phase 3
    • Phase 4
    • IIT
  • Financing
  • Manufacturing
  • Regulatory
    • FTD
    • BTD
    • IND
    • NDA/BLA
    • Approvals
  • Deals
    • M&A
    • Partnerships
  • Events
    • Conferences
    • Forums
    • Workshops
  • Companies
Close

Search

Subscribe
BioPharmChina BioPharmChina BioPharmChina

Covering China's BioPharma industry

BioPharmChina BioPharmChina BioPharmChina

Covering China's BioPharma industry

  • Home
  • Disease Areas
    • Oncology
    • Immunology
    • Autoimmune
    • I&I
    • Metabolic
    • Respiratory
    • Cardiovascular
    • Ophthalmology
    • Neurology
    • Rare Diseases
  • Clinical Trials
    • Phase 1
    • Phase 1/2
    • Phase 2
    • Phase 2/3
    • Phase 3
    • Phase 4
    • IIT
  • Financing
  • Manufacturing
  • Regulatory
    • FTD
    • BTD
    • IND
    • NDA/BLA
    • Approvals
  • Deals
    • M&A
    • Partnerships
  • Events
    • Conferences
    • Forums
    • Workshops
  • Companies
  • Home
  • Disease Areas
    • Oncology
    • Immunology
    • Autoimmune
    • I&I
    • Metabolic
    • Respiratory
    • Cardiovascular
    • Ophthalmology
    • Neurology
    • Rare Diseases
  • Clinical Trials
    • Phase 1
    • Phase 1/2
    • Phase 2
    • Phase 2/3
    • Phase 3
    • Phase 4
    • IIT
  • Financing
  • Manufacturing
  • Regulatory
    • FTD
    • BTD
    • IND
    • NDA/BLA
    • Approvals
  • Deals
    • M&A
    • Partnerships
  • Events
    • Conferences
    • Forums
    • Workshops
  • Companies
Close

Search

Subscribe
Home/Companies/Haisco Pharmaceutical Group
CompaniesI&IImmunology

Haisco Pharmaceutical Group

By Henry Tseng
August 27, 2026 10 Min Read
0

Last updated: August 27, 2026

Company Overview

Haisco Pharmaceutical Group (海思科医药集团股份有限公司; SZSE: 002653) is a commercial-stage Chinese pharmaceutical company engaged in innovative drug discovery and development, manufacturing and commercialization.

Founded in 2000, Haisco initially built its business around specialty and generic medicines before making a major strategic shift toward innovative drug R&D in 2012—the same year it listed on the Shenzhen Stock Exchange. The company has since evolved into an increasingly innovation-driven biopharmaceutical company, with particular strength in small-molecule drug discovery.

Haisco currently focuses primarily on anesthesia/pain, respiratory disease, chronic/metabolic disease, autoimmune/inflammatory disease and oncology, while also developing drugs for rare and complement-mediated diseases. Its pipeline includes small-molecule innovative drugs, biologics and high-end generics.

CompanyHaisco Pharmaceutical Group Co., Ltd.
Chinese name海思科医药集团股份有限公司
Founded2000
Business statusPublic
Stock exchangeShenzhen Stock Exchange
Ticker002653.SZ
Listed2012
Main operating/R&D presenceChengdu, Sichuan, China
Registered/group rootsChina, with operations spanning Sichuan, Tibet, Liaoning and other locations
IndustryPharmaceuticals / Biotechnology
Development stageCommercial-stage
Core therapeutic areasAnesthesia & pain, respiratory, autoimmune/inflammation, metabolic/chronic diseases, oncology, rare/complement diseases
Innovative pipeline27 Class 1 innovative-drug projects disclosed in 2026
Clinical-stage Class 1 projects20+
Marketed Class 1 innovative drugs5 as of July 2026
Core modalitySmall molecules, expanding into biologics, antibodies and ADCs

The company’s principal office disclosed in its latest interim filing is at 136 Baili Road, Wenjiang District, Chengdu, Sichuan Province. Haisco also operates manufacturing facilities in Chengdu/Meishan in Sichuan and Shenyang/Huludao in Liaoning, among other locations. (money.finance.sina.com.cn)


From Generic Drugs to Innovation

A defining moment in Haisco’s history came in 2012, when management began transforming the company from a traditional generic-drug business into an innovative pharmaceutical company.

Haisco established its innovation research organization and substantially increased investment in internally discovered medicines. In recent years, annual R&D investment has consistently exceeded RMB1 billion; in 2024, R&D investment represented approximately 25% of revenue.

That investment is now producing commercial products, late-stage clinical candidates and increasingly valuable international licensing transactions.

Haisco says it currently has more than 20 Class 1 innovative-drug projects in clinical development, spanning anesthesia/pain, respiratory disease, chronic disease, autoimmune disease, oncology and rare diseases.


Therapeutic Areas

Haisco’s innovative pipeline can broadly be divided into five major franchises.

Therapeutic areaMajor programs / approaches
Anesthesia & Pain / CNSCipepofol (HSK3486), HSK21542, HSK16149 and Nav1.8 programs
RespiratoryHSK31858 (DPP1), HSK39004 (PDE3/4), HSK44459 (PDE4B), HSK50042
Autoimmune / InflammationHSK44459, HSK47388, HSK39297 and emerging oral small molecules
Metabolic / Chronic diseaseHSK7653, HSK31679, HSK55879 and other metabolic programs
OncologyHSK42360, HSK46575, HSK41959, HSK46256, HSK47977 and additional precision-oncology programs
Rare / Complement diseaseHSK39297, including PNH, IgA nephropathy and lupus nephritis

Haisco’s historical strength is small-molecule medicinal chemistry, but the company is broadening its technology base. Management said in its 2026 interim report that its emerging large-molecule platform is developing monoclonal antibodies, bispecific/multispecific antibodies and ADCs. (money.finance.sina.com.cn)


Marketed Innovative Drug Portfolio

Haisco reached an important milestone in July 2026 when its fifth internally developed Class 1 innovative drug received Chinese approval.

1. Cipepofol — HSK3486

Cipepofol (HSK3486; 思舒宁® / CYPSEDO) is Haisco’s flagship intravenous anesthetic and one of its most strategically important products.

The drug targets the GABA-A receptor and was developed as a next-generation intravenous anesthetic. It has received multiple approvals in China covering procedural sedation and anesthesia, induction and maintenance of general anesthesia and other uses.

Its biggest international milestone came in May 2026, when the U.S. FDA approved cipepofol for induction of general anesthesia in adults. Haisco announced the approval on June 1.

The approval transformed cipepofol from a primarily Chinese commercial asset into a globally approved innovative drug and represented an important validation of Haisco’s international R&D capabilities.

2. HSK21542 — Anruikefen

Haisco has also commercialized HSK21542, an internally developed analgesic targeting the peripheral κ-opioid receptor.

The company is continuing to expand the product’s indications. In May 2026, China’s NMPA accepted a new marketing application for treatment of postoperative pain, potentially broadening its use across mild, moderate and severe postoperative pain if approved. (money.finance.sina.com.cn)

3. HSK7653 — Beichangping

HSK7653 (倍长平®) is a DPP-4 inhibitor developed for type 2 diabetes and represents an important component of Haisco’s chronic/metabolic disease franchise.

The drug has already reached the Chinese market. Haisco continues to build additional metabolic programs around its established commercial presence in this field.

4. HSK16149 — Keligabalin

HSK16149 (克利加巴林) is another of Haisco’s approved Class 1 innovative drugs, expanding the company’s CNS/pain franchise.

Together with cipepofol and HSK21542, it helps establish anesthesia, analgesia and neuroscience as one of Haisco’s most mature therapeutic franchises.

5. HSK39297 — Sipukopan / Youkupan

One of Haisco’s most important developments of 2026 was the approval of HSK39297 (琥珀酸思普可泮片; 优可盼®).

On July 23, 2026, Chinese regulators approved HSK39297 for adults with paroxysmal nocturnal hemoglobinuria (PNH) who had not previously received complement-inhibitor therapy. It became Haisco’s fifth approved Class 1 innovative drug.

HSK39297 is an oral selective complement Factor B inhibitor designed to block activation of the alternative complement pathway.

Importantly, Haisco is developing the molecule well beyond PNH. Additional programs include:

  • IgA nephropathy — Phase III
  • Lupus nephritis — Phase II
  • Additional PNH regulatory development
  • Generalized myasthenia gravis
  • Age-related macular degeneration

The IgA nephropathy program received Breakthrough Therapy designation in China in 2025. (money.finance.sina.com.cn)


Selected Innovative Drug Pipeline

Haisco’s complete R&D portfolio is substantially larger than the table below. The following highlights the most strategically important clinical and recently commercialized programs.

CandidateTarget / MechanismMajor indication(s)Current status*
Cipepofol (HSK3486)GABA-AAnesthesia/sedationMarketed China & U.S.; additional indications in development
HSK21542Peripheral κ-opioid receptorPain / pruritusMarketed; postoperative-pain NDA accepted
HSK7653DPP-4Type 2 diabetesMarketed
HSK16149CNS/pain mechanismNeuropathic painMarketed
HSK39297Complement Factor BPNHMarketed – China
HSK39297Complement Factor BIgA nephropathyPhase III
HSK39297Complement Factor BLupus nephritisPhase II
HSK31858DPP1Non-CF bronchiectasisPhase III
HSK31858DPP1AsthmaPhase II
HSK39004PDE3/4COPDPhase III
HSK44459PDE4BIPF / progressive pulmonary fibrosisPhase III
HSK44459PDE4BBehçet’s / AD / psoriasisPhase II
HSK47388Oral IL-23 inhibitor peptidePsoriasis / UC / PsAPhase II development
HSK31679Metabolic small moleculeMASH/NASHPhase III
HSK55879MetabolicType 2 diabetes / obesityPhase I
HSK42360BRAF paradox breakerAdvanced solid tumorsPhase I / I-II combinations
HSK46575Precision oncologyProstate cancerPhase I / Ib-II
HSK41959Precision oncologyMTAP-deleted tumorsPhase I development
HSK46256OncologySolid tumorsPhase I
HSK47977OncologySolid tumorsPhase I
HSK50042AntifibroticIdiopathic/progressive pulmonary fibrosisPhase II
HSK45030Small moleculeMuscular dystrophyPhase I
HSK60002Small moleculeInflammatory diseaseIND cleared

*Development status reflects publicly disclosed information available through August 27, 2026; individual assets may have different stages for different indications.

Haisco’s official pipeline categorizes R&D into CNS, respiratory/inflammatory/autoimmune disease, oncology and cardiometabolic disease. (en.haisco.com)


Major Late-Stage Pipeline Opportunities

Click the image to enlarge

HSK31858 — DPP1 Inhibitor

HSK31858 is an oral, selective DPP1 inhibitor targeting inflammatory respiratory disease.

Its lead indication is non-cystic fibrosis bronchiectasis, where the Chinese program has advanced into Phase III. Phase II development is also underway in asthma and chronic airway inflammatory disease associated with mucus hypersecretion. (money.finance.sina.com.cn)

The molecule is internationally partnered with Chiesi Group, which licensed development, manufacturing and commercialization rights outside Greater China in 2023. (chiesi.com)

HSK39004 — PDE3/4 Inhibitor

HSK39004 is another strategically important respiratory asset. It is a dual PDE3/PDE4 inhibitor being developed for COPD.

Haisco is developing both inhaled suspension and dry-powder formulations. By the first half of 2026, both formulations had entered Phase III development in China, while the dry-powder formulation had been included in China’s Breakthrough Therapy program. (money.finance.sina.com.cn)

International rights outside Greater China were licensed to AirNexis Therapeutics in January 2026.

HSK44459 — PDE4B Inhibitor

HSK44459 illustrates how Haisco increasingly develops individual molecules across multiple therapeutic areas.

Two Phase III programs are underway in idiopathic pulmonary fibrosis and progressive pulmonary fibrosis. Haisco is simultaneously evaluating HSK44459 in autoimmune/inflammatory diseases including Behçet’s disease, atopic dermatitis, psoriasis and inflammatory bowel disease. (money.finance.sina.com.cn)

HSK47388 — Oral IL-23 Program

HSK47388 is an oral IL-23 inhibitor peptide being developed for inflammatory diseases.

Phase I studies demonstrated pharmacokinetic and pharmacodynamic findings that supported progression into Phase II development for psoriasis and ulcerative colitis. The molecule received a U.S. FDA IND clearance in June 2025. (en.haisco.com)

On August 19, 2026, Haisco announced Chinese clinical clearance for another indication, psoriatic arthritis, further expanding the potential franchise.


Latest Clinical and Commercial Developments

Haisco has had an unusually active 2026.

DateDevelopmentSignificance
Aug. 26, 2026Preclinical autoimmune asset licensed to Sentivera>$1.5B potential transaction value
Aug. 19, 2026HSK47388 new PsA indication clearedExpands oral IL-23 franchise
Aug. 13, 2026HSK60002 clinical trial approvedAdds inflammatory-disease program
Jul. 23, 2026HSK39297 / Youkupan approved for PNHHaisco’s 5th Class 1 innovative drug
Jun. 23, 2026HSK42360 + HSK39297 licensed to NuvectisExpands oncology/complement programs globally
Jun. 2026HSK31679 Phase III initiatedAdvances metabolic/MASH franchise
Jun. 1, 2026Cipepofol U.S. FDA approval announcedFirst major U.S. approval for Haisco-originated innovation
Jun. 1, 2026Lilly collaboration announcedUp to five discovery programs
Apr. 2026AbbVie pain collaborationGlobalizes Nav1.8 portfolio
Jan. 2026HSK39004 licensed to AirNexisMajor COPD out-licensing transaction

Financial Position and Funding

Haisco differs significantly from a venture-backed clinical-stage biotech. It is a profitable, publicly traded commercial pharmaceutical company that can fund R&D through operating revenue while increasingly generating substantial licensing income.

Its 2026 first-half results, released on August 27, show how rapidly this model is evolving.

Financial metricH1 2026YoY change
RevenueRMB3.096 billion+54.7%
Net profit attributable to shareholdersRMB851.2 million+427.0%
Adjusted net profitRMB752.2 million+324.2%
Operating cash flowRMB760.6 million+117.6%
R&D investmentRMB729.1 million+46.8%

Haisco said the sharp revenue increase was driven in part by higher technology-service revenue associated with new overseas licensing projects. (money.finance.sina.com.cn)

This means Haisco’s financing model increasingly has three engines:

commercial drug sales + internally generated operating cash + global licensing/BD revenue.

That combination gives the company substantially greater financial flexibility than a typical clinical-stage Chinese biotech.


Global Partnerships and Licensing Strategy

International business development has become one of the most important elements of Haisco’s strategy.

During the first half of 2026 alone, Haisco disclosed four transactions with aggregate potential value exceeding US$6 billion, involving AirNexis, AbbVie, Lilly and Nuvectis. (money.finance.sina.com.cn)

The August Sentivera transaction has pushed the potential value of Haisco’s announced 2026 BD transactions even higher.

PartnerProgramTerritory / structureEconomics
Sentivera TherapeuticsPreclinical oral autoimmune/inflammation assetEx-Greater China license~$75.9M upfront + up to $1.46B milestones + ≤10% royalties
Eli LillyUp to 5 small-molecule programsDiscovery/research collaborationUp to $87M upfront/near-term + $2.967B milestones + royalties
AbbVieNav1.8 pain programsEx-Greater China license$30M upfront + >$700M potential milestones + royalties
Nuvectis PharmaHSK42360 + HSK39297Ex-China/global territory licenses$40M upfront/near-term + up to $1.421B milestones + royalties
AirNexis TherapeuticsHSK39004Ex-Greater China$108M upfront + up to $955M milestones + royalties
Chiesi GroupHSK31858Ex-Greater ChinaUpfront + milestones + royalties

Lilly Collaboration

Haisco’s June 2026 agreement with Eli Lilly is especially notable because it is broader than a conventional single-asset licensing deal.

Haisco will conduct discovery and early development work for up to five targets selected by Lilly. Depending on the program, Lilly will receive either global rights or rights outside Greater China.

Haisco is eligible for up to $87 million in upfront and near-term payments, up to $2.967 billion in subsequent milestones, plus tiered royalties.

The deal effectively validates Haisco’s small-molecule discovery platform itself—not simply one particular drug.

AbbVie Pain Partnership

In April 2026, Haisco entered an exclusive licensing agreement with AbbVie covering novel selective Nav1.8 inhibitors for pain.

AbbVie received development, manufacturing and commercialization rights outside Greater China. Haisco receives a $30 million upfront payment, potentially more than $700 million in milestones and tiered royalties. (prnewswire.com)

Nuvectis Partnership

In June, Haisco licensed two programs to Nuvectis Pharma:

HSK42360 — a BRAF “paradox breaker” inhibitor for oncology; and

HSK39297 — the Factor B inhibitor now approved in China for PNH.

Nuvectis obtained HSK42360 rights outside Greater China and HSK39297 rights outside Greater China, India and certain Southeast Asian territories. (prnewswire.com)

AirNexis Partnership

In January 2026, Haisco licensed HSK39004 to AirNexis Therapeutics outside Greater China.

The transaction carries a potential value of $1.063 billion, including a $108 million upfront consideration, up to $955 million in milestones and royalties. Part of the upfront consideration was structured as equity in AirNexis. (static.cninfo.com.cn)


Latest Deal: Sentivera Therapeutics

The newest addition to Haisco’s international partnership portfolio was announced August 26, 2026.

Haisco granted U.S.-based Sentivera Therapeutics exclusive rights outside Greater China to develop, manufacture and commercialize an internally discovered, preclinical-stage oral small-molecule autoimmune/inflammatory drug. Haisco has not publicly identified the molecule in its announcement.

The financial structure is notable:

ComponentPotential value
Cash upfront$40M
Sentivera equity received~$35.9M
Total upfront consideration~$75.9M
Potential milestonesUp to $1.46B
RoyaltiesUp to 10%, tiered
Additional economicsShare of potential sublicensing income

The equity component gives Haisco approximately 17.5% of Sentivera, providing potential participation in the longer-term value of the licensee in addition to conventional milestone and royalty economics. (finance.sina.com.cn)


Haisco’s Emerging Business Model

Haisco’s evolution can be summarized as:

Generic & specialty pharma → China innovative pharma → global innovative biopharma + technology licensor

The company now combines three businesses.

1. Commercial pharmaceuticals.
Five internally developed Class 1 innovative drugs have reached the Chinese market, alongside Haisco’s larger established pharmaceutical portfolio.

2. Proprietary R&D.
Haisco has built a pipeline of approximately 27 Class 1 innovative-drug projects, including more than 20 clinical-stage programs, with multiple Phase III assets.

3. Global innovation licensing.
Haisco is increasingly monetizing assets before global commercialization through partnerships with multinational pharmaceutical companies and U.S. biotechnology companies.

This third component is becoming particularly important. Licensing revenue contributed materially to the company’s 54.7% first-half 2026 revenue growth, while partnerships simultaneously transfer part of the cost and risk of overseas clinical development to international partners. (money.finance.sina.com.cn)


Outlook

Haisco appears to have reached an important transition point.

The company’s original innovative-drug strategy, initiated around 2012, has now produced five approved Class 1 innovative drugs, including cipepofol, which achieved U.S. FDA approval in 2026. HSK39297’s approval gives Haisco a foothold in rare/complement disease, while HSK31858, HSK39004, HSK44459 and HSK31679 provide several additional late-stage opportunities.

At the same time, international licensing has emerged as a significant source of validation and potential capital. Deals involving Lilly, AbbVie, AirNexis, Nuvectis, Chiesi and Sentivera demonstrate external interest across several independent Haisco discovery programs rather than reliance on one flagship molecule.

The Lilly agreement is particularly significant because it extends the relationship from asset licensing into drug discovery itself, with Haisco responsible for discovering and advancing molecules against as many as five Lilly-selected targets.

Financially, Haisco is also in a stronger position than many emerging Chinese biotechnology companies. Its commercial business is generating revenue and operating cash flow, while licensing deals provide substantial upfront and potential milestone income. During H1 2026, revenue reached RMB3.10 billion, attributable net profit RMB851 million and R&D investment RMB729 million. (money.finance.sina.com.cn)

The major question for the next several years will therefore be whether Haisco can translate this unusually broad pipeline and increasingly successful “China discovery → global licensing” model into a sustainable global biopharmaceutical franchise.

With multiple Phase III programs, five marketed innovative medicines, a U.S.-approved anesthetic, an expanding large-molecule platform and more than US$7 billion in potential 2026 BD transaction value based on announced deal economics, Haisco is increasingly moving beyond its roots as a domestic Chinese pharmaceutical company and positioning itself as a global innovation-driven drug developer and licensing partner. (finance.sina.com.cn)

COMPANY NEWS

References

  1. Haisco Pharmaceutical – Official Website
  2. Haisco – R&D Pipeline
  3. Haisco – 2026 Interim Results and Corporate News
  4. Haisco – HSK39297 / Youkupan PNH Approval
  5. Haisco – Cipepofol U.S. FDA Approval
  6. Haisco – Lilly Collaboration
  7. Haisco – HSK39004 / AirNexis Licensing Agreement
  8. Chiesi – HSK31858 Licensing Agreement
  9. Nuvectis Pharma
  10. Haisco – Corporate Operations and Manufacturing Footprint

Tags:

AutoimmuneImmunology
Other Articles
Previous

Akeso, Inc.

Next

Biokin Pharmaceutical

No Comment! Be the first one.

Leave a Reply Cancel reply

Your email address will not be published. Required fields are marked *

2026 H2 AbbVie China Partnering Day
2026 Global XDC Innovation Conference

Welcome to BioPharmChina, a dedicated news and information portal covering the rapidly evolving biotechnology and biopharmaceutical industry in China.

Get the latest news in China's BioPharma industry delivered straight to your inbox.

Latest Articles

  • Inno Medicine Secures Nearly $110M+ to Advance Targeted Nanomedicines for Atherosclerosis and Glioma
  • Unike Biopharma Raises Tens of Millions of RMB to Advance Long-Acting Protein and Peptide Drug Platform
  • 1cBio Licenses PARP1 Inhibitor OC-3 to Lee’s Pharm in $27 Million Asia Deal
  • Lumiere Therapeutics Raises Over RMB 100 Million to Advance Epigenetic Editing Therapies
  • Windward Bio’s WIN378 Delivers Positive Phase 2 Asthma Data as Twice-Yearly Anti-TSLP Antibody Moves Into Phase 3

Info

    About

    Privacy Policy

    Terms of Use

    Newsletter

    Contact

    Contact

    Email
    contact@biopharmchina.com

    Location
    San Francisco, CA, USA

    • X
    • Facebook
    Copyright 2026 — BioPharmChina. All rights reserved.