Accord BioPharma
Accord BioPharma is the U.S. specialty division of Intas Pharmaceuticals, commercializing FDA-approved biosimilars and specialty therapies in oncology, immunology, and critical care for healthcare providers, payers, and patients across the United States.
- Company typePrivate
- Founded2021
- HeadquartersDurham, United States
- Headcount101–250
- GTM typeB2B
- OfferingHardware or Manufacturing
What Accord BioPharma does
Accord BioPharma, Inc. is the U.S. specialty pharmaceutical division of India-based Intas Pharmaceuticals, Ltd., founded in 2021 and headquartered in Raleigh, North Carolina. The company develops, acquires, and commercializes FDA-approved biosimilars and specialty therapies targeting oncology, immunology, and critical care indications. Its commercial portfolio includes six FDA-approved biosimilars: UDENYCA (pegfilgrastim-cbqv, acquired from Coherus BioSciences), HERCESSI (trastuzumab-strf), IMULDOSA (ustekinumab-srlf), OSVYRTI and JUBEREQ (denosumab-desu), FILKRI (filgrastim-laha), and IMMGOLIS/IMMGOLIS INTRI (golimumab-sldi), plus the specialty pharmaceutical CAMCEVI (leuprolide) for advanced prostate cancer.
The company targets oncologists, urologists, rheumatologists, and gastroenterologists through field sales representatives, healthcare provider engagement, and distribution/GPO partnerships. It distributes through specialty pharmacy networks including a captive Accord Specialty Pharmacy, and has secured preferred formulary status with major payers Cigna Healthcare and Express Scripts. The company pursues aggressive biosimilar pricing strategies, exemplified by IMULDOSA launching at a 92% discount to STELARA reference pricing, paired with patient support infrastructure via the AccordCares program (co-pay assistance, benefits investigation, prior authorization support) and the AccordConnects mobile application for HCP inventory management.
Revenue derives from one-time product sales of FDA-approved biosimilar and specialty pharmaceutical products in the U.S. market, with strategic plans to expand to 20 biosimilar launches by 2030. The company recently expanded its geographic footprint through an October 2025 licensing agreement extending BAT2506 (golimumab biosimilar) rights to Canada. Revenue figures are not publicly disclosed.
Accord BioPharma firmographics
Firmographics- Name
- Accord BioPharma
- Legal name
- Accord BioPharma, Inc.
- Website
- https://accordbiopharma.com
- Company type
- Private
- Founded year
- 2021
- Operating status
- Operating
- Headcount range
- 101–250 employees
- Short description
- Accord BioPharma is the U.S. specialty division of Intas Pharmaceuticals, commercializing FDA-approved biosimilars and specialty therapies in oncology, immunology, and critical care for healthcare providers, payers, and patients across the United States.
- Ownership category
- akta.pro rank
Accord BioPharma industry classification
Industry- Product category
- Specialty Biopharmaceuticals / Biosimilars
- NAICS
- Biological Product (except Diagnostic) Manufacturing (325414), Pharmaceutical Preparation Manufacturing (325412), Drugs and Druggists' Sundries Merchant Wholesalers (424210)
- SIC
- Pharmaceutical Preparations (2834), Biological Products, (No Disgnostic Substances) (2836)
- akta.pro primary industry
- Specialty Care Pharmaceuticals (HLAIAAAB)
- akta.pro secondary industries
- Monoclonal Antibody (mAb) Biosimilars (HLAIAFAA), Immunology & Inflammation Pharmaceuticals (HLAIAAAD), Oncology Biosimilars (HLAAAHAG)
Keywords
Where Accord BioPharma is headquartered
LocationHeadquarters
- HQ city
- Durham
- HQ country
- United States
- HQ region
- North America
Offices1 record
Markets served
Accord BioPharma business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Supply Chain, Technology or R&D, Marketing or Sales, Personnel, Operations
Revenue model
- Pharmaceutical Product Sales: Accord BioPharma generates revenue through the sale of FDA-approved biosimilar and specialty pharmaceutical products in the U.S. market, including oncology supportive care, immunology, and critical care therapies.
Pricing tiers
| Model | Billing | Price |
|---|---|---|
| Other | Multi-year contract | $0 co-pay program for eligible patients |
| Unit Pricing | Multi-year contract | IMULDOSA Prefilled Syringes - 92% discount from STELARA |
| Unit Pricing | Multi-year contract | IMULDOSA Vials - 30% discount from STELARA |
Go-to-market motion2 records
Distribution channels4 records
Marketing channels8 records
Accord BioPharma product offering
Product offeringCore offering
Accord BioPharma is the U.S. specialty pharmaceutical and biosimilars division of Intas Pharmaceuticals. It acquires, develops, and commercializes FDA-approved biosimilars and specialty therapies in oncology, immunology, and critical care, including the proprietary ready-to-inject leuprolide product CAMCEVI, and biosimilars referencing reference biologics such as STELARA, Neulasta, NEUPOGEN, Herceptin, Prolia/Xgeva, and Simponi/Simponi Aria. Its portfolio is sold through specialty pharmacies, distribution/GPO partners, and payers, and is complemented by patient and HCP support programs (AccordCares, AccordConnects).
Product overview
Accord BioPharma is a U.S. specialty pharmaceutical division of Intas Pharmaceuticals focused on developing, acquiring, and commercializing biosimilars and specialty therapies in oncology, immunology, and critical care. Their portfolio consists of FDA-approved biosimilars including IMULDOSA (ustekinumab), FILKRI (filgrastim), HERCESSI (trastuzumab), UDENYCA (pegfilgrastim), OSVYRTI and JUBEREQ (denosumab), and IMMGOLIS/IMMGOLIS INTRI (golimumab). The portfolio is complemented by the specialty pharmaceutical CAMCEVI (leuprolide) for advanced prostate cancer. These products are supported by patient and provider support programs including AccordCares and AccordConnects. The company aims to launch 20 biosimilar products by 2030.
Differentiator
Problem solved
Functional benefit
Brands
- AccordCares: Patient support program offering co-pay assistance, patient assistance, benefits investigation, prior authorization support, billing and coding information, and alternate coverage identification for eligible patients.
- AccordConnects
Products and services
- CAMCEVI (leuprolide) 42mg injectable emulsion Injectable emulsion for treatment of adult patients with advanced prostate cancer; first ready-to-inject sterile formulation of leuprolide mesylate for subcutaneous injection, every-six-months dosing via a prefilled syringe.
- IMULDOSA (ustekinumab-srlf) Biosimilar to STELARA (ustekinumab) for moderate to severe plaque psoriasis, active psoriatic arthritis, Crohn's disease, and ulcerative colitis in adults and pediatric patients 6 years and older; available as prefilled syringes (45mg/0.5mL, 90mg/mL) and vials (130mg/26mL).
- UDENYCA (pegfilgrastim-cbqv) Biosimilar to Neulasta (pegfilgrastim) for reducing the incidence of infection (febrile neutropenia) in patients with non-myeloid malignancies receiving myelosuppressive anti-cancer drugs; available in three administration options (autoinjector, on-body injector, and prefilled syringe).
- HERCESSI (trastuzumab-strf) Biosimilar to Herceptin (trastuzumab) for HER2-overexpressing breast cancer and metastatic gastric cancer.
- FILKRI (filgrastim-laha) Biosimilar to NEUPOGEN (filgrastim) approved for cancer patients receiving myelosuppressive chemotherapy, acute myeloid leukemia patients, bone marrow transplant recipients, severe chronic neutropenia patients, and patients exposed to myelosuppressive radiation.
- OSVYRTI (denosumab-desu) Biosimilar to Prolia (denosumab) for treatment of postmenopausal women with osteoporosis at high risk for fracture, men with osteoporosis, glucocorticoid-induced osteoporosis, bone loss from androgen deprivation therapy for prostate cancer, and bone loss from adjuvant aromatase inhibitor therapy for breast cancer.
- JUBEREQ (denosumab-desu) Biosimilar to Xgeva (denosumab) for prevention of skeletal-related events in patients with multiple myeloma and bone metastases from solid tumors, giant cell tumor of bone, and hypercalcemia of malignancy refractory to bisphosphonate therapy.
- IMMGOLIS (golimumab-sldi) First FDA-approved biosimilar to Simponi (golimumab) for treating adults with moderately to severely active rheumatoid arthritis and ulcerative colitis; designated interchangeable for both indications.
- IMMGOLIS INTRI (golimumab-sldi) First FDA-approved biosimilar to Simponi Aria (golimumab) for treating adults with moderately to severely active rheumatoid arthritis and ulcerative colitis; designated interchangeable for both indications.
- AccordCares Patient support program offering Co-pay Assistance, Patient Assistance, Benefits Investigation, Prior Authorization, Billing and Coding Information, and Alternate Coverage Identification for eligible patients prescribed Accord BioPharma medicines.
- AccordConnects Mobile application designed to help healthcare providers manage in-practice inventory of CAMCEVI and access clinical information.
Quantifiable outcome
- IMULDOSA reduces cost by 92% compared to STELARA reference product
- +4 more outcomes
Companies that use Accord BioPharma
Customer profileNamed customers4 records
Segments4 records
Ideal customer profiles3 records
Accord BioPharma technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature1 record
Accord BioPharma partnerships and signals
Strategic signalPartnerships
Seven partnerships are on record, tiered core and minor.
- Coherus BioSciences, Inc.coreAcquisition of UDENYCA (pegfilgrastim-cbqv) franchise from Coherus BioSciences, including UDENYCA prefilled syringe, autoinjector, and on-body injector products. Key Coherus employees across Sales, Marketing, Finance, Supply Chain, and Quality joined Accord BioPharma to ensure supply and services continuity.
- Bio-Thera SolutionscoreFebruary 2025 exclusive U.S. commercialization and license agreement for BAT2506, a golimumab biosimilar candidate referencing Simponi. Bio-Thera maintains responsibility for development, manufacturing, and supply while Accord holds exclusive rights to commercialize in the U.S. This partnership was expanded in October 2025 to include Canada commercialization rights.
- Foresee Pharmaceuticals, Co. LTDcoreCAMCEVI is a registered trademark of Foresee Pharmaceuticals used under a license with Accord BioPharma. CAMCEVI (leuprolide) 42 mg injectable emulsion was developed by Foresee and licensed to Accord for U.S. commercialization.
- ZERO Prostate CancerminorPartnership with leading national nonprofit working to end prostate cancer and help all who are impacted, to create change at community level and beyond through the PRO.STATE of Mind campaign.
- StoryMDminorPartnership with StoryMD to provide physicians and patients compelling and personally curated content for advanced prostate cancer at the point-of-care through StoryMD's platform.
- Accord Specialty PharmacyminorIndependent specialty pharmacy based in Central Florida named finalist in MMIT's Retail Specialty Pharmacy Patient Choice Awards. Provides personalized, patient-centered specialty pharmacy services.
- Intas Pharmaceuticals, Ltd.coreAccord BioPharma is the U.S. specialty division of Intas Pharmaceuticals. Intas provides manufacturing capabilities, regulatory expertise, and global operational support. Accord BioPharma leverages Intas' 40+ years of global expertise in oncology, immunology, and critical care.
Scale indicators6 records
Recent moves9 records
Expansion highlights6 records
Accord BioPharma competitors and assessment
Company assessmentDirect peers
- Coherus BioSciences: Direct biosimilar competitor; sold its UDENYCA franchise to Accord BioPharma in April 2025. Competes in pegfilgrastim and other oncology supportive care biosimilars, providing a like-for-like strategic and operational benchmark.
- Biocon Biologics: Global biosimilar developer and commercializer with strong oncology and immunology biosimilar portfolio, including products referencing trastuzumab, pegfilgrastim, and insulin. Competes directly with Accord across multiple molecule references.
- Alvotech: Pure-play biosimilar developer with a portfolio spanning oncology, immunology, and ophthalmology biosimilars including ustekinumab, adalimumab, and aflibercept. Competes head-to-head with Accord in the U.S. biosimilar market.
- Celltrion: Korean biopharmaceutical company and one of the world's leading biosimilar developers with multiple FDA-approved biosimilars including infliximab, rituximab, trastuzumab, and bevacizumab. Direct competitor across the biosimilar space.
- Samsung Bioepis: Joint venture between Samsung Biologics and Biogen developing biosimilars in immunology, oncology, and ophthalmology including etanercept, infliximab, adalimumab, trastuzumab, and ranibizumab. Direct biosimilar competitor.
- Amneal Pharmaceuticals: U.S. specialty and generics pharmaceutical company with a growing biosimilars business (e.g., pegfilgrastim) and overlapping focus on oncology, immunology, and critical care therapeutic categories where Accord BioPharma competes.
Broad incumbents
- Sandoz (Novartis): Global leader in biosimilars and generics with the largest biosimilar portfolio in the industry. Sandoz competes broadly across multiple biosimilar categories including oncology supportive care and immunology that overlap with Accord's portfolio.
- Viatris: Global healthcare company with a biosimilar portfolio including pegfilgrastim, trastuzumab, and rituximab. Competes with Accord in oncology biosimilars while operating a much broader specialty, generic, and branded pharma business.
- Pfizer (Hospira): Through its Hospira acquisition and continued investment, Pfizer is a major biosimilar player with approved biosimilars across infliximab, rituximab, trastuzumab, and oncology supportive care. Operates as part of Pfizer's broader biopharmaceutical portfolio.
Regional players
- Fresenius Kabi: Global healthcare company expanding its U.S. biosimilars portfolio including pegfilgrastim. While headquartered in Germany, its U.S. operations directly compete with Accord in oncology supportive care biosimilars.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat5 records
Key risks5 records
Key highlights7 records
Customer concentration
Accord BioPharma social profiles
Digital presenceAccord BioPharma financial estimates
Financial estimateRevenue estimate
Valuation estimate
Accord BioPharma leadership team
Management profileNumber of profiles
Profiles1 record
Accord BioPharma funding detail
Funding detailFunding overview
Funding rounds
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Accord BioPharma 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 Accord BioPharma
What does Accord BioPharma do?
Accord BioPharma is the U.S. specialty pharmaceutical and biosimilars division of Intas Pharmaceuticals. It acquires, develops, and commercializes FDA-approved biosimilars and specialty therapies in oncology, immunology, and critical care, including the proprietary ready-to-inject leuprolide product CAMCEVI, and biosimilars referencing reference biologics such as STELARA, Neulasta, NEUPOGEN, Herceptin, Prolia/Xgeva, and Simponi/Simponi Aria. Its portfolio is sold through specialty pharmacies, distribution/GPO partners, and payers, and is complemented by patient and HCP support programs (AccordCares, AccordConnects).
Is Accord BioPharma a public or private company?
Accord BioPharma is a private company. It is classified as corporate owned and is currently operating.
When was Accord BioPharma founded?
Accord BioPharma was founded in 2021. It employs 101 to 250 people.
Where is Accord BioPharma based?
Accord BioPharma is headquartered in Durham, United States, in the North America region.
How does Accord BioPharma make money?
One revenue line is on record: pharmaceutical Product Sales.
Who are Accord BioPharma's main competitors?
Direct peers on record are Coherus BioSciences, Biocon Biologics, Alvotech, Celltrion, Samsung Bioepis and Amneal Pharmaceuticals. Broad incumbents are Sandoz (Novartis), Viatris and Pfizer (Hospira). Fresenius Kabi is listed as a regional player.
Does Accord BioPharma have an API?
No public API is recorded for Accord BioPharma.
What industry is Accord BioPharma in?
Accord BioPharma's product category is Specialty Biopharmaceuticals / Biosimilars. Its primary akta.pro industry code is HLAIAAAB, Specialty Care Pharmaceuticals, with a secondary code of HLAIAFAA, Monoclonal Antibody (mAb) Biosimilars. Its NAICS code is 325414 and its SIC code is 2834.