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// BIOSPECTRUM ASIA
https://www.biospectrumasia.com/news/25/24283/metoject-subcutaneous-injection-pen-launches-in-japan-for-rheumatic-arthritis-treatment.html
13 Sep 2023
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// PRNEWSWIRE
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04 Aug 2021
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12 Jul 2021
// GLOBENEWSWIRE
https://www.globenewswire.com/news-release/2021/07/12/2261295/0/en/Medexus-Pharmaceuticals-and-medac-GmbH-enter-into-Licensing-Agreement-for-First-in-Class-Conditioning-Agent-Treosulfan-in-Canada.html
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12914
Submission : 1998-03-17
Status : Active
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24562
Submission : 2010-12-27
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24562
Submission : 2010-12-27
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12914
Submission : 1998-03-17
Status : Active
Type : II
Details:
Metoject subcutaneous injection pen (methotrexate) works by inhibiting dihydrofolic acid reductase enzyme. It is approved for the treatment of rheumatoid arthritis.
Lead Product(s): Methotrexate
Therapeutic Area: Immunology Brand Name: Metoject
Study Phase: ApprovedProduct Type: Small molecule
Recipient: Eisai
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable February 15, 2024
Lead Product(s) : Methotrexate
Therapeutic Area : Immunology
Highest Development Status : Approved
Recipient : Eisai
Deal Size : Not Applicable
Deal Type : Not Applicable
Metoject® Subcutaneous Injection Pen Approved in Japan for methotrexate Treatment
Details : Metoject subcutaneous injection pen (methotrexate) works by inhibiting dihydrofolic acid reductase enzyme. It is approved for the treatment of rheumatoid arthritis.
Brand Name : Metoject
Molecule Type : Small molecule
Upfront Cash : Not Applicable
February 15, 2024
Details:
Under the agreement, UroGen will develop a next-generation novel mitomycin-based formulation, UGN-103, UroGen’s RTGel® technology combined with medac’s licensed mitomycin, for urothelial cancers.
Lead Product(s): Mitomycin
Therapeutic Area: Oncology Brand Name: UGN-103
Study Phase: PreclinicalProduct Type: Small molecule
Sponsor: UroGen Pharma
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Licensing Agreement January 17, 2024
Lead Product(s) : Mitomycin
Therapeutic Area : Oncology
Highest Development Status : Preclinical
Partner/Sponsor/Collaborator : UroGen Pharma
Deal Size : Undisclosed
Deal Type : Licensing Agreement
Merck Announces Positive Data for V116, a 21-Valent Pneumococcal Vaccine for Adults
Details : Under the agreement, UroGen will develop a next-generation novel mitomycin-based formulation, UGN-103, UroGen’s RTGel® technology combined with medac’s licensed mitomycin, for urothelial cancers.
Brand Name : UGN-103
Molecule Type : Small molecule
Upfront Cash : Undisclosed
January 17, 2024
Details:
Primary endpoint of ACR20 response* at 12 weeks was 59.6% in Metoject (Methotrexate) group versus 51.0% in oral MTX group, indicating comparable efficacy. Adverse drug reaction incidence rates in this trial were 25.0% in the Metoject group and 34.0% in the oral MTX group.
Lead Product(s): Methotrexate
Therapeutic Area: Immunology Brand Name: Metoject
Study Phase: ApprovedProduct Type: Small molecule
Sponsor: Eisai
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable September 26, 2022
Lead Product(s) : Methotrexate
Therapeutic Area : Immunology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : Eisai
Deal Size : Not Applicable
Deal Type : Not Applicable
Metoject® Subcutaneous Injection Syringe (Methotrexate) Approved in Japan for Rheumatoid Arthriti...
Details : Primary endpoint of ACR20 response* at 12 weeks was 59.6% in Metoject (Methotrexate) group versus 51.0% in oral MTX group, indicating comparable efficacy. Adverse drug reaction incidence rates in this trial were 25.0% in the Metoject group and 34.0% in t...
Brand Name : Metoject
Molecule Type : Small molecule
Upfront Cash : Not Applicable
September 26, 2022
Details:
Under the terms of the agreement, medac receives an exclusive license to commercialize oNKord® (GTA002) in the EU, the UK and further European countries for acute myeloid leukemia (AML) and multiple myeloma (MM) patients.
Lead Product(s): GTA002,Cyclophosphamide,Fludarabine Phosphate
Therapeutic Area: Oncology Brand Name: oNKord
Study Phase: Phase I/ Phase IIProduct Type: Cell and Gene therapy
Recipient: Glycostem Therapeutics
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Licensing Agreement August 01, 2022
Lead Product(s) : GTA002,Cyclophosphamide,Fludarabine Phosphate
Therapeutic Area : Oncology
Highest Development Status : Phase I/ Phase II
Recipient : Glycostem Therapeutics
Deal Size : Undisclosed
Deal Type : Licensing Agreement
Details : Under the terms of the agreement, medac receives an exclusive license to commercialize oNKord® (GTA002) in the EU, the UK and further European countries for acute myeloid leukemia (AML) and multiple myeloma (MM) patients.
Brand Name : oNKord
Molecule Type : Cell and Gene therapy
Upfront Cash : Undisclosed
August 01, 2022
Details:
Antibody part of SYD985 (trastuzumab duocarmazine) binds to HER2 on surface of cancer cell and the ADC is internalized by cell. After proteolytic cleavage of linker, the inactive cytotoxin is activated and DNA damage is induced, resulting in tumor cell death.
Lead Product(s): (vic-) Trastuzumab Duocarmazine
Therapeutic Area: Oncology Brand Name: SYD985
Study Phase: Phase IIIProduct Type: Large molecule
Recipient: Byondis
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable July 18, 2022
Details : Antibody part of SYD985 (trastuzumab duocarmazine) binds to HER2 on surface of cancer cell and the ADC is internalized by cell. After proteolytic cleavage of linker, the inactive cytotoxin is activated and DNA damage is induced, resulting in tumor cell d...
Brand Name : SYD985
Molecule Type : Large molecule
Upfront Cash : Not Applicable
July 18, 2022
Details:
Study found event-free survival and overall survival superior after Trecondyv (treosulfan) compared to RIC busulfan, also found non-relapse mortality lower in treosulfan arm than busulfan arm.
Lead Product(s): Treosulfan,Fludarabine Phosphate
Therapeutic Area: Oncology Brand Name: Trecondyv
Study Phase: ApprovedProduct Type: Small molecule
Recipient: Medexus Pharmaceuticals
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable June 06, 2022
Lead Product(s) : Treosulfan,Fludarabine Phosphate
Therapeutic Area : Oncology
Highest Development Status : Approved
Recipient : Medexus Pharmaceuticals
Deal Size : Not Applicable
Deal Type : Not Applicable
Treosulfan Pivotal Study Results Published
Details : Study found event-free survival and overall survival superior after Trecondyv (treosulfan) compared to RIC busulfan, also found non-relapse mortality lower in treosulfan arm than busulfan arm.
Brand Name : Trecondyv
Molecule Type : Small molecule
Upfront Cash : Not Applicable
June 06, 2022
Details:
Treosulfan will be marketed in Canada under the brand name Trecondyv® and indicated in combination with fludarabine as part of a conditioning treatment prior to allogeneic hematopoietic stem cell transplantation (“allo-HSCT”).
Lead Product(s): Treosulfan,Fludarabine Phosphate
Therapeutic Area: Oncology Brand Name: Trecondyv
Study Phase: ApprovedProduct Type: Small molecule
Sponsor: Medexus Pharmaceuticals
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Licensing Agreement July 12, 2021
Lead Product(s) : Treosulfan,Fludarabine Phosphate
Therapeutic Area : Oncology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : Medexus Pharmaceuticals
Deal Size : Undisclosed
Deal Type : Licensing Agreement
Details : Treosulfan will be marketed in Canada under the brand name Trecondyv® and indicated in combination with fludarabine as part of a conditioning treatment prior to allogeneic hematopoietic stem cell transplantation (“allo-HSCT”).
Brand Name : Trecondyv
Molecule Type : Small molecule
Upfront Cash : Undisclosed
July 12, 2021
Details:
Medac intends to leverage its strong, existing commercial infrastructure in the United States to address the underserved allo-HSCT market through its commercialization of treosulfan.
Lead Product(s): Treosulfan,Fludarabine Phosphate
Therapeutic Area: Oncology Brand Name: Trecondi
Study Phase: ApprovedProduct Type: Small molecule
Sponsor: Medexus Pharmaceuticals
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Licensing Agreement February 02, 2021
Lead Product(s) : Treosulfan,Fludarabine Phosphate
Therapeutic Area : Oncology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : Medexus Pharmaceuticals
Deal Size : Undisclosed
Deal Type : Licensing Agreement
Medexus and Medac Enter Into a License Agreement for Treosulfan, in the United States
Details : Medac intends to leverage its strong, existing commercial infrastructure in the United States to address the underserved allo-HSCT market through its commercialization of treosulfan.
Brand Name : Trecondi
Molecule Type : Small molecule
Upfront Cash : Undisclosed
February 02, 2021
Details:
Medac’s sales representatives will begin offering the adalimumab biosimilar IDACIO® as an additional therapy option to the rheumatologists and dermatologists they work with.
Lead Product(s): Adalimumab
Therapeutic Area: Immunology Brand Name: Undisclosed
Study Phase: ApprovedProduct Type: Large molecule
Sponsor: Fresenius Kabi AG
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Agreement May 28, 2020
Lead Product(s) : Adalimumab
Therapeutic Area : Immunology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : Fresenius Kabi AG
Deal Size : Undisclosed
Deal Type : Agreement
Fresenius Kabi Enters Marketing Agreement For Biosimilar Product
Details : Medac’s sales representatives will begin offering the adalimumab biosimilar IDACIO® as an additional therapy option to the rheumatologists and dermatologists they work with.
Brand Name : Undisclosed
Molecule Type : Large molecule
Upfront Cash : Undisclosed
May 28, 2020
Regulatory Info :
Registration Country : Italy
Dosage Form : Film-Coated Tablets
Brand Name : AMBRISENTAN MEDAC
Dosage Strength : 10 mg
Packaging : 30 UNITS 10 MG - ORAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Film-Coated Tablets
Brand Name : AMBRISENTAN MEDAC
Dosage Strength : 5 mg
Packaging : 30 UNITS 5 MG - ORAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
MEDAC GESELLSCHAFT FUR KLINISCHE SPEZIALPRAPARATE MBH
Dosage Form : Bcg Bacillus Calmette An...
Brand Name : Bcg
Dosage Strength : 1 vial groun suspe int...
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Norway
MEDAC GESELLSCHAFT FUR KLINISCHE SPEZIALPRAPARATE MBH
Dosage Form : Powder and liquid to int...
Brand Name : BCG-Medac
Dosage Strength :
Packaging : Set
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Italy
MEDAC GESELLSCHAFT FUR KLINISCHE SPEZIALPRAPARATE MBH
Dosage Form : Bcg Bacillus Calmette An...
Brand Name : Bcg
Dosage Strength : 1 vial groun suspe int...
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
MEDAC GESELLSCHAFT FUR KLINISCHE SPEZIALPRAPARATE MBH
Dosage Form : Bendamustina 25Mg 5 Unit...
Brand Name : Bendamustina
Dosage Strength : 5 VIALS EV 25 mg 2.5 m...
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
MEDAC GESELLSCHAFT FUR KLINISCHE SPEZIALPRAPARATE MBH
Dosage Form : Bendamustina 100Mg 5 Uni...
Brand Name : Bendamustina
Dosage Strength : 5 VIALS EV 100 mg 2,5 ...
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
MEDAC GESELLSCHAFT FUR KLINISCHE SPEZIALPRAPARATE MBH
Dosage Form : Capecitabine 500Mg 120 U...
Brand Name : Capecitabine
Dosage Strength : 120 cpr riv 500 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
MEDAC GESELLSCHAFT FUR KLINISCHE SPEZIALPRAPARATE MBH
Dosage Form : Capecitabine 300Mg 60 Un...
Brand Name : Capecitabine
Dosage Strength : 60 cpr riv 300 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Film Coated Tablet
Brand Name : CAPECITABINE MEDAC
Dosage Strength : 150 mg
Packaging : 60 UNITS 150 MG - ORAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Film-Coated Tablets
Dosage Strength : 10 mg
Packaging : 30 UNITS 10 MG - O...
Brand Name : AMBRISENTAN MEDAC
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Film-Coated Tablets
Dosage Strength : 5 mg
Packaging : 30 UNITS 5 MG - OR...
Brand Name : AMBRISENTAN MEDAC
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
MEDAC GESELLSCHAFT FUR KLINISCHE SPEZIALPRAPARATE MBH
Dosage Form : Bcg Bacillus Calmette And Guer...
Dosage Strength : 1 vial groun suspe intraves...
Packaging :
Brand Name : Bcg
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
MEDAC GESELLSCHAFT FUR KLINISCHE SPEZIALPRAPARATE MBH
Dosage Form : Bcg Bacillus Calmette And Guer...
Dosage Strength : 1 vial groun suspe intraves...
Packaging :
Brand Name : Bcg
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Norway
MEDAC GESELLSCHAFT FUR KLINISCHE SPEZIALPRAPARATE MBH
Dosage Form : Powder and liquid to intravesi...
Dosage Strength :
Packaging : Set
Brand Name : BCG-Medac
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Italy
MEDAC GESELLSCHAFT FUR KLINISCHE SPEZIALPRAPARATE MBH
Dosage Form : Bendamustina 100Mg 5 Units Par...
Dosage Strength : 5 VIALS EV 100 mg 2,5 mg/ml
Packaging :
Brand Name : Bendamustina
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
MEDAC GESELLSCHAFT FUR KLINISCHE SPEZIALPRAPARATE MBH
Dosage Form : Bendamustina 25Mg 5 Units Pare...
Dosage Strength : 5 VIALS EV 25 mg 2.5 mg/ml
Packaging :
Brand Name : Bendamustina
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
MEDAC GESELLSCHAFT FUR KLINISCHE SPEZIALPRAPARATE MBH
Dosage Form : Capecitabine 500Mg 120 Unita' ...
Dosage Strength : 120 cpr riv 500 mg
Packaging :
Brand Name : Capecitabine
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
MEDAC GESELLSCHAFT FUR KLINISCHE SPEZIALPRAPARATE MBH
Dosage Form : Capecitabine 150Mg 60 Units Or...
Dosage Strength : 60 cpr riv 150 mg
Packaging :
Brand Name : Capecitabine
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Film Coated Tablet
Dosage Strength : 500 mg
Packaging : 120 UNITS 500 MG -...
Brand Name : CAPECITABINE MEDAC
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
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