Only Regulatory Products (API/FDF), Drugs in Developments and News are Updated on this Virtual Booth
Update your Virtual Booth on PharmaCompass, ask us
About
Not Confirmed
Not Confirmed
17-20 March, 2025
Pharma, Lab & Chemical...Pharma, Lab & Chemical Expo
Not Confirmed
Not Confirmed
03-05 January, 2025
Not Confirmed
Not Confirmed
07-09 January, 2025
List your booth number for exhibitions, ask us
CONTACT DETAILS
Upload your Marketing & Sales content on your company Virtual Booth, click HERE.
Events
Webinars & Exhibitions
Industry Trade Show
Not Confirmed
17-20 March, 2025
Pharma, Lab & Chemical...Pharma, Lab & Chemical Expo
Industry Trade Show
Not Confirmed
03-05 January, 2025
Industry Trade Show
Not Confirmed
07-09 January, 2025
Digital content
INTERVIEW #SpeakPharma
[Sponsored by another company]https://www.pharmacompass.com/speak-pharma/translational-pharmaceutics-our-flagship-platform-for-drug-development-empowers-our-clients-with-unparalleled-flexibility
VLOG #PharmaReel
[Sponsored by another company]DATA COMPILATION #PharmaFlow
[Sponsored by another company]https://www.pharmacompass.com/radio-compass-blog/bms-j-j-bayer-lead-25-000-pharma-layoffs-in-2024-amylyx-fibrogen-kronos-bio-hit-by-trial-failures-cash-crunch
16 Nov 2023
// REUTERS
https://www.reuters.com/business/healthcare-pharmaceuticals/fda-panel-urges-acrotech-speed-up-study-cancer-drugs-2023-11-16/
24 Nov 2022
// INDIANPHARMAPOST
https://www.indianpharmapost.com/news/evive-enters-license-agreement-with-acrotech-biopharma-to-commercialize-ryzneuta-in-us-13335
24 Sep 2021
// Z. Brennan ENDPTS
https://endpts.com/fdas-cancer-drug-advisors-will-review-2-more-dangling-accelerated-approvals-for-multiple-myeloma-leukemia/
26 Apr 2021
// BUSINESSWIRE
https://www.businesswire.com/news/home/20210426005126/en/Acrotech-Biopharma-Announces-the-Publication-of-Data-From-a-Phase-1-Study-of-BELEODAQ%C2%AE-belinostat-Combined-With-Standard-CHOP-Bel-CHOP-in-Patients-With-Previously-Untreated-Peripheral-T-cell-Lymphoma
26 Apr 2021
// BUSINESSWIRE
Details:
The partnership aims for the manufacturing and advancement of iTolerance's Streptavidin-FasL (SA-FasL) fusion protein, a crucial component of the proprietary iTOL-100 platform technology towards first in human clinical study for lead program, iTOL-102.
Lead Product(s): Pralatrexate
Therapeutic Area: Oncology Brand Name: Folotyn
Study Phase: ApprovedProduct Type: Small molecule
Sponsor: CASI Pharmaceuticals
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Licensing Agreement August 01, 2023
Lead Product(s) : Pralatrexate
Therapeutic Area : Oncology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : CASI Pharmaceuticals
Deal Size : Undisclosed
Deal Type : Licensing Agreement
Details : The partnership aims for the manufacturing and advancement of iTolerance's Streptavidin-FasL (SA-FasL) fusion protein, a crucial component of the proprietary iTOL-100 platform technology towards first in human clinical study for lead program, iTOL-102.
Brand Name : Folotyn
Molecule Type : Small molecule
Upfront Cash : Undisclosed
August 01, 2023
Details:
The new Agreement grants Acrotech a royalty-free license to belinostat in all other territories including the United States, Canada, Mexico, and India.
Lead Product(s): Belinostat
Therapeutic Area: Oncology Brand Name: Undisclosed
Study Phase: ApprovedProduct Type: Small molecule
Recipient: Onxeo
Deal Size: $6.6 million Upfront Cash: $6.6 million
Deal Type: Agreement April 06, 2020
Lead Product(s) : Belinostat
Therapeutic Area : Oncology
Highest Development Status : Approved
Recipient : Onxeo
Deal Size : $6.6 million
Deal Type : Agreement
Details : The new Agreement grants Acrotech a royalty-free license to belinostat in all other territories including the United States, Canada, Mexico, and India.
Brand Name : Undisclosed
Molecule Type : Small molecule
Upfront Cash : $6.6 million
April 06, 2020
Regulatory Info : RX
Registration Country : USA
Dosage Form : POWDER;INTRAVENOUS
Brand Name : BELEODAQ
Dosage Strength : 500MG/VIAL
Packaging :
Approval Date : 2014-07-03
Application Number : 206256
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : POWDER;INTRAVENOUS
Brand Name : KHAPZORY
Dosage Strength : 300MG/VIAL
Packaging :
Approval Date : 2018-10-19
Application Number : 211226
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : POWDER;INTRAVENOUS
Brand Name : KHAPZORY
Dosage Strength : 175MG/VIAL
Packaging :
Approval Date : 2018-10-19
Application Number : 211226
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : FUSILEV
Dosage Strength : EQ 175MG BASE/17.5ML (...
Packaging :
Approval Date : 2011-04-29
Application Number : 20140
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : POWDER;INTRAVENOUS
Brand Name : FUSILEV
Dosage Strength : EQ 50MG BASE/VIAL
Packaging :
Approval Date : 2008-03-07
Application Number : 20140
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : FUSILEV
Dosage Strength : EQ 250MG BASE/25ML (EQ...
Packaging :
Approval Date : 2011-04-29
Application Number : 20140
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : POWDER;INTRAVENOUS
Brand Name : EVOMELA
Dosage Strength : EQ 50MG BASE/VIAL
Packaging :
Approval Date : 2016-03-10
Application Number : 207155
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : FOLOTYN
Dosage Strength : 20MG/ML (20MG/ML)
Packaging :
Approval Date : 2009-09-24
Application Number : 22468
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : FOLOTYN
Dosage Strength : 40MG/2ML (20MG/ML)
Packaging :
Approval Date : 2009-09-24
Application Number : 22468
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE, LIPOSOMAL;IN...
Brand Name : MARQIBO KIT
Dosage Strength : 5MG/5ML (1MG/ML)
Packaging :
Approval Date : 2012-08-09
Application Number : 202497
Regulatory Info : DISCN
Registration Country : USA
RLD : Yes
TE Code :
Dosage Form : POWDER; INTRAVENOUS
Proprietary Name : BELEODAQ
Dosage Strength : 500MG/VIAL
Approval Date : 2014-07-03
Application Number : 206256
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : POWDER; INTRAVENOUS
Proprietary Name : KHAPZORY
Dosage Strength : 175MG/VIAL
Approval Date : 2018-10-19
Application Number : 211226
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : POWDER; INTRAVENOUS
Proprietary Name : KHAPZORY
Dosage Strength : 300MG/VIAL
Approval Date : 2018-10-19
Application Number : 211226
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : POWDER; INTRAVENOUS
Proprietary Name : FUSILEV
Dosage Strength : EQ 50MG BASE/VIAL
Approval Date : 2008-03-07
Application Number : 20140
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SOLUTION; INTRAVENOUS
Proprietary Name : FUSILEV
Dosage Strength : EQ 175MG BASE/17.5ML (EQ...
Approval Date : 2011-04-29
Application Number : 20140
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SOLUTION; INTRAVENOUS
Proprietary Name : FUSILEV
Dosage Strength : EQ 250MG BASE/25ML (EQ 1...
Approval Date : 2011-04-29
Application Number : 20140
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : POWDER; INTRAVENOUS
Proprietary Name : EVOMELA
Dosage Strength : EQ 50MG BASE/VIAL
Approval Date : 2016-03-10
Application Number : 207155
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SOLUTION; INTRAVENOUS
Proprietary Name : FOLOTYN
Dosage Strength : 20MG/ML (20MG/ML)
Approval Date : 2009-09-24
Application Number : 22468
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : SOLUTION; INTRAVENOUS
Proprietary Name : FOLOTYN
Dosage Strength : 40MG/2ML (20MG/ML)
Approval Date : 2009-09-24
Application Number : 22468
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : INJECTABLE, LIPOSOMAL; INTRAVE...
Proprietary Name : MARQIBO KIT
Dosage Strength : 5MG/5ML (1MG/ML)
Approval Date : 2012-08-09
Application Number : 202497
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
ABOUT THIS PAGE
LOOKING FOR A SUPPLIER?