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Accord BioPharma

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uuid000652f

Namestring
Accord BioPharma
Legal namestring
Accord BioPharma, Inc.
Company typeenum
Private
Founded yearint
2021
Descriptiontext

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.

Short descriptiontext

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.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersDurham, United States
HQ citystring
Durham
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
biosimilar pharmaceuticals, oncology therapeutics, immunology biologics, specialty pharmaceuticals, G-CSF supportive care
Industry4 codes
1Specialty Care Pharmaceuticals
CodeHLAIAAABPrimaryYes
2Monoclonal Antibody (mAb) Biosimilars
CodeHLAIAFAAPrimaryNo
3Immunology & Inflammation Pharmaceuticals
CodeHLAIAAADPrimaryNo
4Oncology Biosimilars
CodeHLAAAHAGPrimaryNo
NAICS code3 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Pharmaceutical Preparation Manufacturing325412
  • Drugs and Druggists' Sundries Merchant Wholesalers424210
SIC code2 codes
  • Pharmaceutical Preparations2834
  • Biological Products, (No Disgnostic Substances)2836
Product category
Specialty Biopharmaceuticals / Biosimilars
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model1 record
1Pharmaceutical Product Sales
TypeOne Time License
Description

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.

accordbiopharma.com
Marketing channels8 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels4 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Supply Chain, Technology or R&D, Marketing or Sales, Personnel, Operations
Pricing details3 tiers
1$0 co-pay program for eligible patients
ModelOtherBilling cadenceMulti-year contract
Notes

Accord BioPharma offers $0 co-pay program for eligible patients prescribed IMULDOSA to maximize patient access to biosimilar therapies.

biospace.com
2IMULDOSA Prefilled Syringes - 92% discount from STELARA
ModelUnit PricingBilling cadenceMulti-year contract
Notes

Prefilled syringes represent majority of ustekinumab market presentations and are priced at lowest WAC among all branded ustekinumab biosimilars at 92% discount from reference product STELARA.

accordbiopharma.com
3IMULDOSA Vials - 30% discount from STELARA
ModelUnit PricingBilling cadenceMulti-year contract
Notes

Vial formulation offers 30% discount from STELARA reference pricing for intravenous infusion administration.

accordbiopharma.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 2 records shown
1AccordCares
Description

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.

accordbiopharma.com
+1 more record
Core offering1 text field

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).

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • IMULDOSA reduces cost by 92% compared to STELARA reference product
+4 more records
Product overview1 text field

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.

Product and service11 records
1CAMCEVI (leuprolide) 42mg injectable emulsion
CategorySpecialty Pharmaceutical (Prostate Cancer / GnRH Agonist)
Description

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.

2IMULDOSA (ustekinumab-srlf)
CategoryBiosimilar (Immunology)
Description

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).

3UDENYCA (pegfilgrastim-cbqv)
CategoryBiosimilar (Oncology Supportive Care / G-CSF)
Description

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).

4HERCESSI (trastuzumab-strf)
CategoryBiosimilar (Oncology / HER2-targeted)
Description

Biosimilar to Herceptin (trastuzumab) for HER2-overexpressing breast cancer and metastatic gastric cancer.

5FILKRI (filgrastim-laha)
CategoryBiosimilar (Oncology Supportive Care / G-CSF)
Description

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.

6OSVYRTI (denosumab-desu)
CategoryBiosimilar (Bone Health)
Description

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.

7JUBEREQ (denosumab-desu)
CategoryBiosimilar (Bone Health / Oncology Supportive Care)
Description

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.

8IMMGOLIS (golimumab-sldi)
CategoryBiosimilar (Immunology / Anti-TNF)
Description

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.

9IMMGOLIS INTRI (golimumab-sldi)
CategoryBiosimilar (Immunology / Anti-TNF)
Description

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.

10AccordCares
CategoryPatient Support Program
Description

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.

11AccordConnects
CategoryMobile Application (HCP Tool)
Description

Mobile application designed to help healthcare providers manage in-practice inventory of CAMCEVI and access clinical information.

Scale indicator6 records

Each record includes

Type, Value, Description, Source

Partnership7 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-04-01
Description

Acquisition 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.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-02-01
Description

February 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.

Strategic tierCoreTypeOEM/ Whitelabel/ Licensing Partner
Description

CAMCEVI 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.

Strategic tierMinorTypeGTM or Marketing Partner
Description

Partnership 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.

Strategic tierMinorTypeGTM or Marketing Partner
Description

Partnership 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.

Strategic tierMinorTypeChannel Partner/ Reseller/ Distributor
Description

Independent specialty pharmacy based in Central Florida named finalist in MMIT's Retail Specialty Pharmacy Patient Choice Awards. Provides personalized, patient-centered specialty pharmacy services.

Strategic tierCoreTypeOthers
Description

Accord 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.

Recent move9 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

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.

TypeDirect peer
Description

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.

TypeDirect peer
Description

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.

TypeDirect peer
Description

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.

TypeBroad incumbent
Description

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.

TypeDirect peer
Description

Joint venture between Samsung Biologics and Biogen developing biosimilars in immunology, oncology, and ophthalmology including etanercept, infliximab, adalimumab, trastuzumab, and ranibizumab. Direct biosimilar competitor.

TypeBroad incumbent
Description

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.

TypeBroad incumbent
Description

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.

TypeDirect peer
Description

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.

TypeRegional player
Description

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

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers4 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment4 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature1 record

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles1 record

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Accord BioPharma

Specialty Biopharmaceuticals / Biosimilarsaccordbiopharma.com

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.

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

  • Biosimilar pharmaceuticals
  • Oncology therapeutics
  • Immunology biologics
  • Specialty pharmaceuticals
  • G-CSF supportive care

Where Accord BioPharma is headquartered

Location

Headquarters

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

  1. 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

ModelBillingPrice
OtherMulti-year contract$0 co-pay program for eligible patients
Unit PricingMulti-year contractIMULDOSA Prefilled Syringes - 92% discount from STELARA
Unit PricingMulti-year contractIMULDOSA Vials - 30% discount from STELARA

Go-to-market motion2 records

Distribution channels4 records

Marketing channels8 records

Accord BioPharma product offering

Product offering

Core 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 profile

Named customers4 records

Segments4 records

Ideal customer profiles3 records

Accord BioPharma technology and API

Technology

Technology 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 signal

Partnerships

Seven partnerships are on record, tiered core and minor.

  • Coherus BioSciences, Inc.coreStrategic or Co-development Partner · 1 April 2025Acquisition 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 SolutionscoreStrategic or Co-development Partner · 1 February 2025February 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. LTDcoreOEM/ Whitelabel/ Licensing PartnerCAMCEVI 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 CancerminorGTM or Marketing PartnerPartnership 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.
  • StoryMDminorGTM or Marketing PartnerPartnership 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 PharmacyminorChannel Partner/ Reseller/ DistributorIndependent 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.coreOthersAccord 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 assessment

Direct 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

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Accord BioPharma financial estimates

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Accord BioPharma leadership team

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Profiles1 record

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Accord BioPharma M&A and investment

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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.

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TrendHunter.comShort-Acting Cancer BiosimilarsAccord BioPharma has launched FILKRI, a short-acting biosimilar to Neupogen, in the U.S. to help restore neutrophil levels in chemotherapy patients. The FDA-approved medication joined the company's existing long-acting UDENYCA treatment and features a permanent Medicare and Medicaid billing code effective October 1. This expansion provides clinicians with greater dosing flexibility and supports Accord's strategy to strengthen its presence in the competitive biosimilar market.PharmExecPharmaceutical Executive Daily: FDA Approves EnnumoThe FDA approved Ennumo, a biosimilar to Neulasta developed by Accord BioPharma, for use in reducing febrile neutropenia incidence and increasing survival in specific cancer and radiation exposure patients. Concurrently, Chemomab Therapeutics and Scipher Medicine announced a merger valued at $150 million to combine antibody technology with AI platforms, while Teva secured global licensing rights from Polpharma Biologics for an Ocrevus biosimilar. Cencora analyst Alina Chesnokova highlighted the industry shift toward cold chain-dependent specialty therapies requiring new commercialization strategies.Drug Store NewsAccord BioPharma introduces denosumab biosimilarsAccord BioPharma, the U.S. specialty division of Intas Pharmaceuticals, has launched two denosumab biosimilars — Osvyrti and Jubereq — both FDA-approved as interchangeable biosimilars to Amgen's Prolia and Xgeva respectively. The launch marks Accord BioPharma's first products developed and manufactured end-to-end by its parent entity, representing a significant milestone for the company's biosimilar portfolio. Osvyrti received approval for multiple osteoporosis indications including treatment of postmenopausal women with osteoporosis at high fracture risk and bone mass increase in men receiving androgen deprivation therapy.PR NewswireAccord BioPharma Announces Commercial Availability of Denosumab Biosimilars OSVYRTI® (denosumab-desu) and JUBEREQ® (denosumab-desu)Accord BioPharma, Inc., the U.S. specialty division of Intas Pharmaceuticals, announced on July 23, 2026, the commercial launch of two denosumab biosimilars—OSVYRTI® (interchangeable with Prolia®) and JUBEREQ® (interchangeable with XGEVA®)—representing the company's first products developed and manufactured end-to-end by its parent entity. The products are priced at WAC of $1,800.41 per 60 mg/mL dose for OSVYRTI and $3,311.75 per 120 mg/1.7 mL dose for JUBEREQ, with both brands achieving Preferred status on Cigna commercial pharmacy benefit drug lists, addressing over $2 billion in annual Medicare Part B denosumab spending. The launch marks Accord BioPharma's evolution as a fully integrated biosimilar company and supports its goal of bringing 20 biosimilars to the U.S. market by 2030.Drug Store NewsAccord BioPharma obtains FDA nod for EnnumoAccord BioPharma has received FDA approval for Ennumo (pegfilgrastim-pccg), a biosimilar referencing Amgen's Neulasta, indicated to decrease infection incidence in cancer patients experiencing febrile neutropenia. With this approval, Accord BioPharma becomes the only company in the United States offering two distinct pegfilgrastim biosimilars, Ennumo and Udenyca, alongside Filkri. The three products collectively form a G-CSF portfolio targeting oncology practices, hospitals, and patients.PR NewswireFDA Approves ENNUMO™ (pegfilgrastim-pccg), Accord BioPharma's Second Pegfilgrastim Biosimilar to NEULASTA® (pegfilgrastim)The FDA approved ENNUMO (pegfilgrastim-pccg), Accord BioPharma's second pegfilgrastim biosimilar referencing Amgen's NEULASTA, for use in decreasing infection incidence in cancer patients undergoing myelosuppressive chemotherapy. With this approval, Accord BioPharma becomes the only company in the U.S. offering two distinct pegfilgrastim biosimilars alongside a filgrastim option, creating the largest G-CSF biosimilar portfolio from a single company. The milestone supports Accord BioPharma's strategic goal of launching 20 biosimilars in the U.S. by 2030, backed by parent company Intas Pharmaceuticals.BioSpaceFDA Approves ENNUMO™ (pegfilgrastim-pccg), Accord BioPharma’s Second Pegfilgrastim Biosimilar to NEULASTA® (pegfilgrastim)The FDA approved ENNUMO (pegfilgrastim-pccg), a biosimilar to NEULASTA, for febrile neutropenia and radiation-induced hematopoietic syndrome. Accord BioPharma now offers two pegfilgrastim biosimilars and a filgrastim biosimilar, aiming to launch 20 biosimilars by 2030.MorningstarFDA Approves ENNUMO™ (pegfilgrastim-pccg), Accord BioPharma's Second Pegfilgrastim Biosimilar to NEULASTA® (pegfilgrastim)The FDA approved ENNUMO (pegfilgrastim-pccg), Accord BioPharma's second pegfilgrastim biosimilar to NEULASTA, for febrile neutropenia and radiation-induced hematopoietic syndrome. The approval gives Accord the most comprehensive G-CSF biosimilar portfolio in the U.S., with two pegfilgrastim options and a filgrastim biosimilar. The company aims to launch 20 biosimilars by 2030.PR NewswireFDA Approves IMMGOLIS™ (golimumab-sldi) and IMMGOLIS INTRI™ (golimumab-sldi), First Biosimilars to Simponi® (golimumab) and Simponi Aria® (golimumab); Accord BioPharma to Lead U.S. CommercializationThe U.S. Food and Drug Administration approved IMMGOLIS™ (golimumab-sldi) and IMMGOLIS INTRI™ (golimumab-sldi), the first biosimilars to Simponi® and Simponi Aria® respectively, for treating adults with moderately to severely active rheumatoid arthritis and ulcerative colitis. Accord BioPharma will exclusively commercialize both products in the United States starting Q4 2026, while Bio-Thera Solutions maintains manufacturing responsibility. The FDA designated both biosimilars interchangeable for rheumatoid arthritis and ulcerative colitis, representing the first golimumab biosimilar options available in the U.S. market.PR NewswireBio-Thera Solutions' Golimumab Biosimilars Receive FDA Approval as First Biosimilars to Simponi® and Simponi Aria®; Accord BioPharma to Commercialize IMMGOLIS™ (golimumab-sldi) and IMMGOLIS INTRI™ (goBio-Thera Solutions and Accord BioPharma announced FDA marketing authorization for IMMGOLIS and IMMGOLIS INTRI, the first approved biosimilars to Simponi and Simponi Aria for treating rheumatoid arthritis and ulcerative colitis. Under a February 2025 exclusive agreement, Bio-Thera handles development, manufacturing, and supply while Accord BioPharma commercializes the products in the United States. This marks the first FDA-approved golimumab biosimilar in the U.S., potentially expanding affordable treatment access for patients with autoimmune conditions.