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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Shanghai Minbiotech is the leading producer of biopharmaceuticals and a variety of high-end generic & innovative drugs.



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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
About the Company : LGM Pharma is a global leader in sourcing APIs, including hard-to-find drug substances, for pharmaceutical and biotech industries. LGM also operates as a full-service drug product ...
Shanghai Minbiotech is the leading producer of biopharmaceuticals and a variety of high-end generic & innovative drugs.
About the Company : Shanghai Minbiotech is specializing in the R&D and production of advanced pharmaceutical intermediates and biological APIs. There are more than 1000 square meters of R&D centers in...
About the Company : BIOTECHNICA DWC LLC has carved a niche for itself in providing value added compliance, regulatory qualification, project management and GDP guidance services to pharma companies al...

About the Company : KinBio is a rapidly growing biopharmaceutical company based in Rehovot, Israel, with its main focus on developing needed therapies as well as offering a wide range of CDMO services...

About the Company : Established in 1997, Nanogen Pharmaceutical Biotechnology JSC has been striving to become a world-class innovative biotechnology company in the pharmaceutical industry. We are pro...

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Methotrexate is a Other Small Molecule drug candidate, which is currently being evaluated in phase III clinical studies for the treatment of Arthritis, Rheumatoid.
Lead Product(s): Methotrexate,Adalimumab
Therapeutic Area: Immunology Brand Name: Undisclosed
Study Phase: Phase IIIProduct Type: Cytotoxic Drug
Sponsor: Regeneron Pharmaceuticals
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable January 10, 2013
Lead Product(s) : Methotrexate,Adalimumab
Therapeutic Area : Immunology
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Regeneron Pharmaceuticals
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : Methotrexate is a Other Small Molecule drug candidate, which is currently being evaluated in phase III clinical studies for the treatment of Arthritis, Rheumatoid.
Product Name : Undisclosed
Product Type : Cytotoxic Drug
Upfront Cash : Inapplicable
January 10, 2013
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Details:
Adalimumab is a Antibody drug candidate, which is currently being evaluated in phase IV clinical studies for the treatment of Uveitis.
Lead Product(s): Adalimumab,Inapplicable
Therapeutic Area: Ophthalmology Brand Name: Undisclosed
Study Phase: Phase IVProduct Type: Antibody, Unconjugated
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable June 10, 2022
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Lead Product(s) : Adalimumab,Inapplicable
Therapeutic Area : Ophthalmology
Highest Development Status : Phase IV
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : Adalimumab is a Antibody drug candidate, which is currently being evaluated in phase IV clinical studies for the treatment of Uveitis.
Product Name : Undisclosed
Product Type : Antibody, Unconjugated
Upfront Cash : Inapplicable
June 10, 2022
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Details:
HUMIRA® is a fully human anti-TNF-α monoclonal antibody, got additional approval for a highdose regimen in adult patients with ulcerative colitis and for a new regimen in pediatric patients.
Lead Product(s): Adalimumab,Inapplicable
Therapeutic Area: Immunology Brand Name: Humira
Study Phase: Approved FDFProduct Type: Antibody, Unconjugated
Sponsor: Eisai
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable September 27, 2021
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Lead Product(s) : Adalimumab,Inapplicable
Therapeutic Area : Immunology
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Eisai
Deal Size : Inapplicable
Deal Type : Inapplicable
Fully Human Anti-TNFα Monoclonal Antibody HUMIRA® Obtains Additional Approval for High-Dose Regi...
Details : HUMIRA® is a fully human anti-TNF-α monoclonal antibody, got additional approval for a highdose regimen in adult patients with ulcerative colitis and for a new regimen in pediatric patients.
Product Name : Humira
Product Type : Antibody, Unconjugated
Upfront Cash : Inapplicable
September 27, 2021
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Details:
HUMIRA (adalimumab) is the first and only subcutaneous biologic treatment option for pediatric patients from 5 years of age with moderately to severely active ulcerative colitis.
Lead Product(s): Adalimumab,Inapplicable
Therapeutic Area: Immunology Brand Name: Humira
Study Phase: Approved FDFProduct Type: Antibody, Unconjugated
Sponsor: Eisai
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable April 24, 2021
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Lead Product(s) : Adalimumab,Inapplicable
Therapeutic Area : Immunology
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Eisai
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : HUMIRA (adalimumab) is the first and only subcutaneous biologic treatment option for pediatric patients from 5 years of age with moderately to severely active ulcerative colitis.
Product Name : Humira
Product Type : Antibody, Unconjugated
Upfront Cash : Inapplicable
April 24, 2021
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Details:
Approval for adalimumab based on results from the pivotal Phase 3 ENVISION I study showing the higher dosage of HUMIRA induced clinical remission in 60 percent of patients at Week 8 and 45 percent of patients, who responded at Week 8, were in remission at Week 52.
Lead Product(s): Adalimumab,Inapplicable
Therapeutic Area: Immunology Brand Name: Humira
Study Phase: Approved FDFProduct Type: Antibody, Unconjugated
Sponsor: Eisai
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable February 24, 2021
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Lead Product(s) : Adalimumab,Inapplicable
Therapeutic Area : Immunology
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Eisai
Deal Size : Inapplicable
Deal Type : Inapplicable
HUMIRA® (adalimumab) Receives FDA Approval to Treat Pediatric Patients Living with Moderately to ...
Details : Approval for adalimumab based on results from the pivotal Phase 3 ENVISION I study showing the higher dosage of HUMIRA induced clinical remission in 60 percent of patients at Week 8 and 45 percent of patients, who responded at Week 8, were in remission a...
Product Name : Humira
Product Type : Antibody, Unconjugated
Upfront Cash : Inapplicable
February 24, 2021
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Details:
Adalimumab is a Antibody drug candidate, which is currently being evaluated in phase III clinical studies for the treatment of Pyoderma Gangrenosum.
Lead Product(s): Adalimumab,Inapplicable
Therapeutic Area: Rare Diseases and Disorders Brand Name: Undisclosed
Study Phase: Phase IIIProduct Type: Antibody, Unconjugated
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable October 17, 2017
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Lead Product(s) : Adalimumab,Inapplicable
Therapeutic Area : Rare Diseases and Disorders
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : Adalimumab is a Antibody drug candidate, which is currently being evaluated in phase III clinical studies for the treatment of Pyoderma Gangrenosum.
Product Name : Undisclosed
Product Type : Antibody, Unconjugated
Upfront Cash : Inapplicable
October 17, 2017
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Details:
Adalimumab is a Antibody drug candidate, which is currently being evaluated in clinical studies for the treatment of Crohn Disease.
Lead Product(s): Adalimumab,Inapplicable
Therapeutic Area: Immunology Brand Name: Undisclosed
Study Phase: UndisclosedProduct Type: Antibody, Unconjugated
Sponsor: waqqas.afif
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable August 24, 2017
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Lead Product(s) : Adalimumab,Inapplicable
Therapeutic Area : Immunology
Highest Development Status : Undisclosed
Partner/Sponsor/Collaborator : waqqas.afif
Deal Size : Inapplicable
Deal Type : Inapplicable
TDM Guided Early Optimization of ADAL in Crohn's Disease
Details : Adalimumab is a Antibody drug candidate, which is currently being evaluated in clinical studies for the treatment of Crohn Disease.
Product Name : Undisclosed
Product Type : Antibody, Unconjugated
Upfront Cash : Inapplicable
August 24, 2017
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Details:
Adalimumab is a Antibody drug candidate, which is currently being evaluated in phase II/ phase III clinical studies for the treatment of Psoriasis.
Lead Product(s): Adalimumab,Methotrexate
Therapeutic Area: Dermatology Brand Name: Undisclosed
Study Phase: Phase II/ Phase IIIProduct Type: Antibody, Unconjugated
Sponsor: Jeffrey J Crowley MD
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable July 14, 2017
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Lead Product(s) : Adalimumab,Methotrexate
Therapeutic Area : Dermatology
Highest Development Status : Phase II/ Phase III
Partner/Sponsor/Collaborator : Jeffrey J Crowley MD
Deal Size : Inapplicable
Deal Type : Inapplicable
MAP Study: Methotrexate and Adalimumab in Psoriasis
Details : Adalimumab is a Antibody drug candidate, which is currently being evaluated in phase II/ phase III clinical studies for the treatment of Psoriasis.
Product Name : Undisclosed
Product Type : Antibody, Unconjugated
Upfront Cash : Inapplicable
July 14, 2017
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Details:
Adalimumab is a Antibody drug candidate, which is currently being evaluated in phase III clinical studies for the treatment of Hidradenitis Suppurativa.
Lead Product(s): Adalimumab,Inapplicable
Therapeutic Area: Dermatology Brand Name: Undisclosed
Study Phase: Phase IIIProduct Type: Antibody, Unconjugated
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable September 19, 2016
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Lead Product(s) : Adalimumab,Inapplicable
Therapeutic Area : Dermatology
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Open-label Study of Adalimumab in Japanese Subjects With Hidradenitis Suppurativa
Details : Adalimumab is a Antibody drug candidate, which is currently being evaluated in phase III clinical studies for the treatment of Hidradenitis Suppurativa.
Product Name : Undisclosed
Product Type : Antibody, Unconjugated
Upfront Cash : Inapplicable
September 19, 2016
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Details:
Adalimumab is a Antibody drug candidate, which is currently being evaluated in phase IV clinical studies for the treatment of Axial Spondyloarthritis.
Lead Product(s): Adalimumab,Inapplicable
Therapeutic Area: Immunology Brand Name: Undisclosed
Study Phase: Phase IVProduct Type: Antibody, Unconjugated
Sponsor: IST GmbH | Hannover Medical School | Improvement by Movement
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable September 13, 2016
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Lead Product(s) : Adalimumab,Inapplicable
Therapeutic Area : Immunology
Highest Development Status : Phase IV
Partner/Sponsor/Collaborator : IST GmbH | Hannover Medical School | Improvement by Movement
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : Adalimumab is a Antibody drug candidate, which is currently being evaluated in phase IV clinical studies for the treatment of Axial Spondyloarthritis.
Product Name : Undisclosed
Product Type : Antibody, Unconjugated
Upfront Cash : Inapplicable
September 13, 2016
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Regulatory Info :
Registration Country : USA
Brand Name : HUMIRA
Dosage Form : SYRINGE
Dosage Strength : 40MG/0.8ML
Packaging :
Approval Date :
Application Number : 125057
Regulatory Info :
Registration Country : USA
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Regulatory Info :
Registration Country : USA
Brand Name : HUMIRA
Dosage Form : VIAL
Dosage Strength : 40MG/0.8ML
Packaging :
Approval Date :
Application Number : 125057
Regulatory Info :
Registration Country : USA
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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Humira
Dosage Form : Solution For Injection
Dosage Strength : 40mg/0.4ml
Packaging :
Approval Date : 2003-04-16
Application Number : 56221
Regulatory Info : Allowed
Registration Country : Switzerland
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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Humira
Dosage Form : Solution For Injection
Dosage Strength : 20mg/0.2ml
Packaging :
Approval Date : 2003-04-16
Application Number : 56221
Regulatory Info : Allowed
Registration Country : Switzerland
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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Humira
Dosage Form : Solution For Injection
Dosage Strength : 80mg/0.8ml
Packaging :
Approval Date : 2003-04-16
Application Number : 56221
Regulatory Info : Allowed
Registration Country : Switzerland
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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Humira
Dosage Form : Injectable Solution
Dosage Strength : 40mg/0.4ml
Packaging :
Approval Date : 2007-03-20
Application Number : 57862
Regulatory Info : Allowed
Registration Country : Switzerland
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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Humira
Dosage Form : Injectable Solution
Dosage Strength : 80mg/0.8ml
Packaging :
Approval Date : 2007-03-20
Application Number : 57862
Regulatory Info : Allowed
Registration Country : Switzerland
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Regulatory Info : Prescription
Registration Country : Estonia
Brand Name : Humira
Dosage Form : Solution For Injection
Dosage Strength : 20mg/0.2ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia
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Regulatory Info : Prescription
Registration Country : Estonia
Brand Name : Humira
Dosage Form : Solution For Injection
Dosage Strength : 40mg/0.4ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia
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Regulatory Info : Prescription
Registration Country : Estonia
Brand Name : Humira
Dosage Form : Solution For Injection
Dosage Strength : 40mg/0.4ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia
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RLD :
TE Code :
Brand Name : HUMIRA
Dosage Form : SYRINGE
Dosage Strength : 40MG/0.8ML
Approval Date :
Application Number : 125057
RX/OTC/DISCN :
RLD :
TE Code :
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RLD :
TE Code :
Brand Name : HUMIRA
Dosage Form : VIAL
Dosage Strength : 40MG/0.8ML
Approval Date :
Application Number : 125057
RX/OTC/DISCN :
RLD :
TE Code :
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RLD :
TE Code :
Brand Name : SIMLANDI
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 40MG/0.4ML
Approval Date :
Application Number : 761299
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : AMJEVITA
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 20MG/0.4ML
Approval Date :
Application Number : 761024
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : IDACIO
Dosage Form : INJECTABLE;SUBCUTANEOUS
Dosage Strength : 40MG/0.8ML
Approval Date :
Application Number : 761255
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : ABRILADA
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 40MG/0.8ML
Approval Date :
Application Number : 761118
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : ABRILADA
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 20MG/0.4ML
Approval Date :
Application Number : 761118
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : ABRILADA
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10MG/0.2ML
Approval Date :
Application Number : 761118
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : HADLIMA
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 40MG/0.8ML
Approval Date :
Application Number : 761059
RX/OTC/DISCN :
RLD :
TE Code :

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RLD :
TE Code :
Brand Name : HYRIMOZ
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 40MG/0.8ML
Approval Date :
Application Number : 761071
RX/OTC/DISCN :
RLD :
TE Code :

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Related Excipient Companies
Dosage Form : Tablet
Grade : Oral
Application : Taste Masking
Excipient Details : Mannitol is used as a filler, bulking agent and taste masking agent in ODT formulations such as tablets.
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Global Sales Information
Main Therapeutic Indication : Immunology
Currency : USD
2020 Revenue in Millions : 19,832
2019 Revenue in Millions : 19,169
Growth (%) : 3
Main Therapeutic Indication : Immunology (Organ Transplant, Arthr...
Currency : USD
2017 Revenue in Millions : 18,427
2016 Revenue in Millions : 16,078
Growth (%) : 15
Main Therapeutic Indication : Immunology
Currency : USD
2021 Revenue in Millions : 20,694
2020 Revenue in Millions : 19,832
Growth (%) : 4
Main Therapeutic Indication : Immunology (Organ Transplant, Arthr...
Currency : USD
2016 Revenue in Millions : 16,078
2015 Revenue in Millions : 14,012
Growth (%) : 15
Main Therapeutic Indication : Immunology (Organ Transplant, Arthr...
Currency : USD
2015 Revenue in Millions : 12,543
2014 Revenue in Millions : 14,012
Growth (%) : 12%
Main Therapeutic Indication : Immunology
Currency : USD
2022 Revenue in Millions : 21,237
2021 Revenue in Millions : 20,694
Growth (%) : 3
Main Therapeutic Indication : Immunology
Currency : USD
2023 Revenue in Millions : 14,404
2022 Revenue in Millions : 21,237
Growth (%) : -32
Main Therapeutic Indication : Immunology
Currency : USD
2024 Revenue in Millions : 8,993
2023 Revenue in Millions : 14,404
Growth (%) : -38
Main Therapeutic Indication : Immunology (Organ Transplant, Arthr...
Currency : USD
2018 Revenue in Millions : 19,936
2017 Revenue in Millions : 18,427
Growth (%) : 8%
Main Therapeutic Indication : Immunology
Currency : USD
2019 Revenue in Millions : 19,169
2018 Revenue in Millions : 19,936
Growth (%) : -4
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Market Place
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Patents & EXCLUSIVITIES
Patent Expiration Date : 2017-02-10
Date Granted : 2002-09-17
Brand Name : HUMIRA
Patent Number : 2243459
Filing Date : 1997-02-10
Strength per Unit : 50 mg / mL (40 mg in 0.8 mL)
Dosage Form : Solution
Human Or VET : Human
Route of Administration : Subcutaneous Injection
Patent Expiration Date : 2017-02-10
Date Granted : 2002-09-17
Patent Expiration Date : 2022-05-10
Date Granted : 2015-02-17
Brand Name : HUMIRA
Patent Number : 2385745
Filing Date : 2002-05-10
Strength per Unit : 50 mg / mL (40 mg in 0.8 mL)
Dosage Form : Solution
Human Or VET : Human
Route of Administration : Subcutaneous Injection
Patent Expiration Date : 2022-05-10
Date Granted : 2015-02-17
Patent Expiration Date : 2023-08-15
Date Granted : 2014-07-22
Brand Name : HUMIRA
Patent Number : 2494756
Filing Date : 2003-08-15
Strength per Unit : 50 mg / mL (40 mg in 0.8 mL)
Dosage Form : Solution
Human Or VET : Human
Route of Administration : Subcutaneous Injection
Patent Expiration Date : 2023-08-15
Date Granted : 2014-07-22
Patent Expiration Date : 2025-04-11
Date Granted : 2015-04-07
Brand Name : HUMIRA
Patent Number : 2847142
Filing Date : 2005-04-11
Strength per Unit : 50 mg / mL (40 mg in 0.8 mL)
Dosage Form : Solution
Human Or VET : Human
Route of Administration : Subcutaneous Injection
Patent Expiration Date : 2025-04-11
Date Granted : 2015-04-07
Patent Expiration Date : 2025-04-11
Date Granted : 2016-11-29
Brand Name : HUMIRA
Patent Number : 2504868
Filing Date : 2005-04-11
Strength per Unit : 50 mg / mL (40 mg in 0.8 mL)
Dosage Form : Solution
Human Or VET : Human
Route of Administration : Subcutaneous Injection
Patent Expiration Date : 2025-04-11
Date Granted : 2016-11-29
Patent Expiration Date : 2025-04-11
Date Granted : 2015-04-07
Brand Name : HUMIRA
Patent Number : 2847142
Filing Date : 2005-04-11
Strength per Unit : 100mg / mL (40mg / 0.4mL)
Dosage Form : SOLUTION
Human Or VET : Human
Route of Administration : SUBCUTANEOUS
Patent Expiration Date : 2025-04-11
Date Granted : 2015-04-07
Patent Expiration Date : 2017-02-10
Date Granted : 2002-09-17
Brand Name : HUMIRA
Patent Number : 2243459
Filing Date : 1997-02-10
Strength per Unit : 100mg / mL (40mg / 0.4mL)
Dosage Form : SOLUTION
Human Or VET : Human
Route of Administration : SUBCUTANEOUS
Patent Expiration Date : 2017-02-10
Date Granted : 2002-09-17
Patent Expiration Date : 2022-05-10
Date Granted : 2015-02-17
Brand Name : HUMIRA
Patent Number : 2385745
Filing Date : 2002-05-10
Strength per Unit : 100mg / mL (40mg / 0.4mL)
Dosage Form : SOLUTION
Human Or VET : Human
Route of Administration : SUBCUTANEOUS
Patent Expiration Date : 2022-05-10
Date Granted : 2015-02-17
Patent Expiration Date : 2031-11-11
Date Granted : 2016-11-22
Brand Name : HUMIRA
Patent Number : 2815689
Filing Date : 2011-11-11
Strength per Unit : 100mg / mL (40mg / 0.4mL)
Dosage Form : SOLUTION
Human Or VET : Human
Route of Administration : SUBCUTANEOUS
Patent Expiration Date : 2031-11-11
Date Granted : 2016-11-22
Patent Expiration Date : 2025-04-11
Date Granted : 2016-11-29
Brand Name : HUMIRA
Patent Number : 2504868
Filing Date : 2005-04-11
Strength per Unit : 100mg / mL (40mg / 0.4mL)
Dosage Form : SOLUTION
Human Or VET : Human
Route of Administration : SUBCUTANEOUS
Patent Expiration Date : 2025-04-11
Date Granted : 2016-11-29
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