Lead Product(s) : AD1208
Therapeutic Area : Oncology
Study Phase : IND Enabling
Sponsor : Stassets Investment
Deal Size : $12.3 million
Deal Type : Series B Financing
Avelos Therapeutics Announces KRW 17 Billion Series B Funding Round
Details : The funding aims to support the Avelos lead product candidate AVS1001, which is being evaluated in the early-stage clinical trials for the treatment of colon cancer and stomach cancer.
Product Name : AD1208
Product Type : Other Small Molecule
Upfront Cash : Undisclosed
May 29, 2024
Lead Product(s) : AD1208
Therapeutic Area : Oncology
Highest Development Status : IND Enabling
Sponsor : Stassets Investment
Deal Size : $12.3 million
Deal Type : Series B Financing
Lead Product(s) : BH3120,Pembrolizumab
Therapeutic Area : Oncology
Study Phase : IND Enabling
Sponsor : Merck & Co
Deal Size : Undisclosed
Deal Type : Collaboration
Hanmi Enters Clinical Trial Collaboration with MSD to Evaluate BH3120 and KEYTRUDA®
Details : The collaboration will support Hanmi in advancing trials for its immuno-oncology drug BH3120 combined with Keytruda in metastatic solid tumors.
Product Name : BH3120
Product Type : Other Large Molecule
Upfront Cash : Undisclosed
April 23, 2024
Lead Product(s) : BH3120,Pembrolizumab
Therapeutic Area : Oncology
Highest Development Status : IND Enabling
Sponsor : Merck & Co
Deal Size : Undisclosed
Deal Type : Collaboration
Lead Product(s) : SLC-3010
Therapeutic Area : Oncology
Study Phase : IND Enabling
Sponsor : GenScript ProBio
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : SLC-3010 selectively stimulates anti-tumor immune response and the efficacy of SLC-3010 in eradication of various types of tumor was thoroughly demonstrated through various in vitro and in vivo experiments.
Product Name : SLC-3010
Product Type : Antibody
Upfront Cash : Inapplicable
August 23, 2022
Lead Product(s) : SLC-3010
Therapeutic Area : Oncology
Highest Development Status : IND Enabling
Sponsor : GenScript ProBio
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : GEN-001,Pembrolizumab
Therapeutic Area : Oncology
Study Phase : IND Enabling
Sponsor : Merck & Co
Deal Size : Undisclosed
Deal Type : Collaboration
Details : Upon the execution of the agreement, Genome will conduct a phase 2 clinical trial to evaluate the safety and efficacy of its immuno-oncology microbiome therapeutic, GEN-001, in combination with MSD’s anti-PD-1 therapy, KEYTRUDA®, in patients with bili...
Product Name : GEN-001
Product Type : Microorganism
Upfront Cash : Undisclosed
March 03, 2022
Lead Product(s) : GEN-001,Pembrolizumab
Therapeutic Area : Oncology
Highest Development Status : IND Enabling
Sponsor : Merck & Co
Deal Size : Undisclosed
Deal Type : Collaboration
Lead Product(s) : PAb001-ADC
Therapeutic Area : Oncology
Study Phase : IND Enabling
Sponsor : Qilu Pharmaceutical
Deal Size : Undisclosed
Deal Type : Licensing Agreement
Qilu Pharmaceutical and Peptron Sign License Agreement for anti-MUC1 ADC
Details : Under the terms of the agreement, Peptron grants Qilu an exclusive global right and license to develop, manufacture, sell, and commercialize PAb001-ADC for the treatment of cancers.
Product Name : PAb001-ADC
Product Type : Antibody-drug Conjugate
Upfront Cash : Undisclosed
April 16, 2021
Lead Product(s) : PAb001-ADC
Therapeutic Area : Oncology
Highest Development Status : IND Enabling
Sponsor : Qilu Pharmaceutical
Deal Size : Undisclosed
Deal Type : Licensing Agreement
Lead Product(s) : KVA12.1
Therapeutic Area : Oncology
Study Phase : IND Enabling
Sponsor : Kineta
Deal Size : Undisclosed
Deal Type : Partnership
Humedix Closes Strategic Investment in US-based Kineta to Boost CMO Business
Details : Humedix has secured certain exclusive distribution rights in Korea for products that are commercialized from Kineta's pipeline currently under development including KVA12.1.
Product Name : KVA12.1
Product Type : Antibody
Upfront Cash : Undisclosed
April 10, 2021
Lead Product(s) : KVA12.1
Therapeutic Area : Oncology
Highest Development Status : IND Enabling
Sponsor : Kineta
Deal Size : Undisclosed
Deal Type : Partnership
Lead Product(s) : EU101
Therapeutic Area : Oncology
Study Phase : IND Enabling
Sponsor : Samsung Biologics
Deal Size : Inapplicable
Deal Type : Inapplicable
Samsung Biologics, National OncoVenture, and Eutilex obtains IND Approval from FDA
Details : Studied by NOV and Eutilex with humanized mice, EU101(NOV1801), effectively eradicated human tumors and showed synergistic anti-tumor activity with immune checkpoint blockade.
Product Name : EU101
Product Type : Antibody
Upfront Cash : Inapplicable
January 27, 2021
Lead Product(s) : EU101
Therapeutic Area : Oncology
Highest Development Status : IND Enabling
Sponsor : Samsung Biologics
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : EU101
Therapeutic Area : Oncology
Study Phase : IND Enabling
Sponsor : National OncoVenture
Deal Size : Inapplicable
Deal Type : Inapplicable
Samsung Biologics, National OncoVenture, and Eutilex Obtain IND Approval from FDA
Details : Studied by NOV and Eutilex with humanized mice, EU101(NOV1801), effectively eradicated human tumors and showed synergistic anti-tumor activity with immune checkpoint blockade.
Product Name : EU101
Product Type : Antibody
Upfront Cash : Inapplicable
January 27, 2021
Lead Product(s) : EU101
Therapeutic Area : Oncology
Highest Development Status : IND Enabling
Sponsor : National OncoVenture
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : BBT-176,Undisclosed
Therapeutic Area : Oncology
Study Phase : IND Enabling
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Bridge Biotherapeutics Announces the IND Clearance of BBT-176, an EGFR TKI for NSCLC, in South Korea
Details : On IND clearance in South Korea, Bridge Biotherapeutics plans to initiate a dose escalation study as the first part of the phase I/II study in Korea to find the maximum tolerable dose of BBT-176.
Product Name : BBT-176
Product Type : Other Small Molecule
Upfront Cash : Inapplicable
July 05, 2020
Lead Product(s) : BBT-176,Undisclosed
Therapeutic Area : Oncology
Highest Development Status : IND Enabling
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
Lead Product(s) : GEN-001,Avelumab
Therapeutic Area : Oncology
Study Phase : IND Enabling
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable
First Anti-Cancer Microbiome Therapeutic Receives FDA IND Clearance in Asia
Details : Genome & Company which sponsor clinical trial of combination therapy of anti-cancer microbiome and anti-PD1/anti-PD-L1 drug receives FDA IND clearance for GEN-001,
Product Name : GEN-001
Product Type : Microorganism
Upfront Cash : Inapplicable
April 20, 2020
Lead Product(s) : GEN-001,Avelumab
Therapeutic Area : Oncology
Highest Development Status : IND Enabling
Sponsor : Inapplicable
Deal Size : Inapplicable
Deal Type : Inapplicable