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PharmAbcine Inc.
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PharmAbcine Inc.

http://www.pharmabcine.com/
Last activity: 15.10.2024
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Categories: BioTechDevelopmentDrugGrowthInvestmentITOwnProductionPublicTechnology
2008년 설립 이후, 차세대 항암 항체신약 개발에 주력해 올린베시맵과 다양한 신약 후보물질의 개발 및 사업화 기반을 구축했습니다.

파멥신은 비면역 scFv 파아지 디스플레이 라이브러리를 활용한 항체 개발 기술과 차세대 이중표적항체 제조기술 그리고 암 줄기세포 라이브러리를 활용한 항체 제조기술 등 혁신적인 바이오 핵심 기술을 보유하고 있습니다.

파멥신은 자체 기술력을 기반으로 임상개발 단계를 진행하고 글로벌 블록버스터 바이오신약 출시를 목표로 합니다. 이를 위해 지속적이고 혁신적인 파이프라인 개발을 통해 대한민국을 대표하는 글로벌 바이오 벤처기업으로 성장해나갈 것입니다.
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Mentions
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Location: South Korea, Daejeon
Employees: 51-200
Phone: 042-863-2017
Founded date: 2008

Investors 4

Mentions in press and media 42

DateTitleDescription
15.10.2024PharmAbcine Announces Safety Approval for 4mg Single-dose Cohort in Phase 1 Clinical Trial of PMC-403 for Neovascular Age-related Macular DegenerationSafety Review Committee (SRC) approves single ascending dose 4mg cohort in Phase 1 trial of PMC-403, preparing for multiple ascending dose 4 mg cohort. PMC-403 is being explored in broader therapeutic areas, including rare vascular disease ...
08.07.2024PharmAbcine Announces Safety Approval for the First Dose Cohort in Phase 1a/b Clinical Trial of PMC-309 in Patients with Advanced or Metastatic Solid TumorsPMC-309 receives safety approval for first dose cohort (0.2mg/kg), and second dose cohort (0.5mg/kg) is currently underway in Australia. DAEJEON, South Korea, July 8, 2024 /PRNewswire/ -- PharmAbcine Inc. (KOSDAQ: 208340ks), a clinical-stag...
02.07.2024PharmAbcine's Phase 1 Clinical Trial of PMC-403 for Neovascular Age-related Macular Degeneration Advances to Both Single-dose of 4mg and Multiple-dose of 3mgSafety Review Committee (SRC) approves single 3mg dose for the third cohort in Phase 1 trial of PMC-403 DAEJEON, South Korea, July 2, 2024 /PRNewswire/ -- PharmAbcine, Inc. ("PharmAbcine" or the "Company") (KOSDAQ: 20834...
01.07.2024PharmAbcine's Phase 1 Clinical Trial of PMC-403 for Neovascular Age-related Macular Degeneration Advances to Both Single-dose of 4mg and Multiple-dose of 3mgSafety Review Committee (SRC) approves single 3mg dose for the third cohort in Phase 1 trial of PMC-403 DAEJEON, South Korea, July 2, 2024 /PRNewswire/ -- PharmAbcine, Inc. ("PharmAbcine" or the "Company") (KOSDAQ: 20834...
27.05.2024Revolutionizing Eye Treatment: The Future of Non-Invasive TherapyThe recent presentation at ARVO 2024 by PharmAbcine's U.S. subsidiary, Wincal Biopharm, has sparked excitement in the medical community. Their innovative eye drop formulations have shown promising results in animal studies, potentially chan...
23.05.2024PharmAbcine's U.S. Subsidiary, Wincal Biopharm, Presented Preclinical Data on Eye Drops from its Proprietary OPC Platform at ARVO 2024Presentation at ARVO 2024 gained attention as Eylea (aflibercept) eye drops demonstrated similar efficacy to intravitreal injections in animal studies. DAEJEON, South Korea, May 23, 2024 /PRNewswire/ -- PharmAbcine, Inc. ("PharmAbcine&...
22.05.2024PharmAbcine's U.S. Subsidiary, Wincal Biopharm, Presented Preclinical Data on Eye Drops from its Proprietary OPC Platform at ARVO 2024Presentation at ARVO 2024 gained attention as Eylea (aflibercept) eye drops demonstrated similar efficacy to intravitreal injections in animal studies. DAEJEON, South Korea , May 22, 2024 /PRNewswire/ -- PharmAbcine, Inc. ("PharmAbcine...
24.01.2024PharmAbcine Announces First Patient Dosed in Phase 1a/b Clinical Trial of PMC-309 in Combination with KEYTRUDA® (pembrolizumab) in Patients with Advanced or Metastatic Solid TumorsInitiation of Phase 1a/b clinical trial exploring MTD, RP2D, safety and tolerability of PMC-309 monotherapy and combination therapy with KEYTRUDA® The clinical trial aims to enroll a total of 67 patients across four institutions in Australi...
23.11.2023PharmAbcine Publishes Study in Science Advances Demonstrating the Potential of PMC-403 in Preclinical Models of Idiopathic Systemic Capillary Leak SyndromeStudy reveals a promising avenue for addressing Idiopathic Systemic Capillary Leak Syndrome (ISCLS, a.k.a. Clarkson Disease) and vessel-related rare disease indications Unique Tie2-activating antibody program, PMC-403, demonstrates efficacy...
09.11.2023PharmAbcine Receives Safety Review Committee Approval to Advance to Dose Level 2 of Clinical Trial of PMC-403 with Neovascular Age-related Macular Degeneration following Dose Level 1 Safety DataSafety Review Committee evaluated dose level 1 safety data of PMC-403 and approved advancing to the higher dose treatment. The starting dose (0.7mg) of PMC-403 showed potential in improving eyesight for neovascular age-related macular degen...
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