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Apollomics, Inc. Appoints Seasoned Healthcare Executive K. Peony Yu, M.D., as Chief Medical Officer

– Fibrogen veteran brings global R&D expertise to Management Team – – Merck KGaA Executive Sophie (Zhengjie) Sun named Senior Vice President, Corporate Development bringing partnership, strategy and commercialization expertise – Foster City, CA, and Hangzhou, China, March 9, 2021 — Apollomics, Inc., an innovative biopharmaceutical company committed to the discovery and development of mono- and […]

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APOLLOMICS, INC ANNOUNCES SUCCESSFUL ENROLLMENT OF FIRST PATIENT INTO PHASE 1 CLINICAL TRIAL OF APL-106 (UPROLESELAN INJECTION) IN CHINA

FOSTER CITY, Calif. and HANGZHOU, ZHEJIANG, CHINA, March 4, 2021, Apollomics, Inc., an innovative biopharmaceutical company committed to the discovery and development of mono- and combination- oncology therapies, today announced that the first patient has been successfully enrolled into a Phase 1 clinical trial of APL-106 (uproleselan injection) for the treatment of adults with relapsed

APOLLOMICS, INC ANNOUNCES SUCCESSFUL ENROLLMENT OF FIRST PATIENT INTO PHASE 1 CLINICAL TRIAL OF APL-106 (UPROLESELAN INJECTION) IN CHINA Read More »

Apollomics, Inc. Licenses a Targeted, Active Checkpoint Control Immunotherapy for Greater China and South Africa

TYG100 utilizes proprietary S-TIR™ technology platform enabling specific B cell and T cell responses against tumor antigens  FOSTER CITY, Calif. and HANGZHOU, ZHEJIANG, CHINA, February 12, 2021 – Apollomics, Inc., an innovative biopharmaceutical company committed to the discovery and development of mono- and combination- oncology therapies, today announced an exclusive license agreement for the development

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Apollomics, Inc. and Iterion Therapeutics Announce Exclusive Collaboration and License Agreement to Develop and Commercialize Tegavivint in Greater China

Agreement will expand clinical development for a potent and selective small molecule targeting TBL1, a downstream target in the Wnt/b-catenin signaling pathway FOSTER CITY, Calif. and HANGZHOU, China and HOUSTON, Texas, February 10, 2021 – Apollomics, Inc., an innovative biopharmaceutical company committed to the discovery and development of mono- and combination- oncology therapies, and Iterion

Apollomics, Inc. and Iterion Therapeutics Announce Exclusive Collaboration and License Agreement to Develop and Commercialize Tegavivint in Greater China Read More »

Apollomics, Inc. and Edison Oncology Announce Licensing Agreement for Novel Protein Tyrosine Kinase Inhibitor Targeting Solid Tumors

– Apollomics licenses worldwide rights (ex-China, Hong Kong and Taiwan) to develop and commercialize EO1001 –  – EO1001 is an irreversible, pan-erbB inhibitor of EGFR (ErbB1), HER2 (ErbB2) and HER4 (ErbB4) – FOSTER CITY, Calif. and HANGZHOU, China and MENLO PARK, CA, February 9, 2021 – Apollomics, Inc., an innovative biopharmaceutical company committed to the

Apollomics, Inc. and Edison Oncology Announce Licensing Agreement for Novel Protein Tyrosine Kinase Inhibitor Targeting Solid Tumors Read More »

APL-106 (uproleselan) Granted Breakthrough Therapy Designation in China for the Treatment of Acute Myeloid Leukemia

Foster City, CA, Hangzhou, China, Gaithersburg, MD,  January 7, 2021 — Apollomics, Inc., an innovative biopharmaceutical company committed to the discovery and development of mono- and combination- oncology therapies, and GlycoMimetics (Nasdaq: GLYC), today announced APL-106 (uproleselan) has been granted Breakthrough Therapy Designation (BTD) from the China National Medical Products Administration (NMPA) Center for Drug Evaluation (CDE)

APL-106 (uproleselan) Granted Breakthrough Therapy Designation in China for the Treatment of Acute Myeloid Leukemia Read More »

APOLLOMICS, INC. RECEIVES CHINA INVESTIGATIONAL NEW DRUG APPROVAL FOR APL-102 TO INITIATE A PHASE 1 STUDY

Foster City, CA, and Hangzhou, China, November 11, 2020 – Apollomics, Inc., an innovative biopharmaceutical company committed to the discovery and development of new tumor-targeting agents and immuno-oncology agents and their combination therapies, today announced that APL-102 has received China Investigational New Drug (IND) approval from the Center for Drug Evaluation (CDE) of the National

APOLLOMICS, INC. RECEIVES CHINA INVESTIGATIONAL NEW DRUG APPROVAL FOR APL-102 TO INITIATE A PHASE 1 STUDY Read More »

Apollomics, Inc. Closes $124 Million Series C Financing

– Financing led by Ping An Capital – – Phase 2 SPARTA Trial for APL-101 Now Enrolling – – Phase 3 Clinical Trial to begin in China for APL-106 (Uproleselan) –  Foster City, CA, and Hangzhou, China, November 6, 2020 — Apollomics, Inc., an innovative biopharmaceutical company committed to the discovery and development of oncology combination

Apollomics, Inc. Closes $124 Million Series C Financing Read More »

Apollomics, Inc. Receives China Investigational New Drug Approval for APL-106 to Initiate a Phase 3 Bridging Study in Acute Myeloid Leukemia

Foster City, CA, and Hangzhou, China, September 27, 2020 — Apollomics, Inc., an innovative biopharmaceutical company committed to the discovery and development of mono- and combination- oncology therapies, today announced APL-106 (uproleselan) has received Investigational New Drug (IND) approval from the China National Medical Products Administration (NMPA) Center for Drug Evaluation (CDE).  This approval enables the

Apollomics, Inc. Receives China Investigational New Drug Approval for APL-106 to Initiate a Phase 3 Bridging Study in Acute Myeloid Leukemia Read More »

Apollomics, Inc. Announces Initiation of SPARTA Phase 2 Clinical Trial for c-MET Inhibitor APL-101

– Trial will evaluate diverse MET dysregulations across broad tumor types – – Focus on non-small cell lung cancer with a mutation that leads to MET exon 14 skipping, and tumors with amplifications and MET fusions, including glioblastoma multiforme – Foster City, CA, and Hangzhou, China, 21 May 2020 — Apollomics, Inc., an innovative biopharmaceutical company

Apollomics, Inc. Announces Initiation of SPARTA Phase 2 Clinical Trial for c-MET Inhibitor APL-101 Read More »