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T-1101 Receives TFDA Approval for Phase II Clinical Trial, Advancing Development Milestone
Taivex announced that its investigational drug T-1101 has received approval from Taiwan’s Food and Drug Administration (TFDA) to initiate Phase II clinical trials. The study will further evaluate the safety and efficacy of T-1101 in patients with neuroendocrine tumors (NET), supporting the path toward future regulatory filings. T-1101 is a first-in-class oral small-molecule inhibitor targeting Hec1/Nek2, designed to treat …

T-1201 Phase I study design present at 2025 ASCO
The 2025 ASCO Annual Meeting will be held from May 30 to June 3 in Chicago, USA. ASCO (American Society of Clinical Oncology) is the world’s largest and most authoritative clinical oncology meeting, bringing together many of the world’s leading oncology experts, and ASCO is an annual research event that publishes clinical oncology results from around the world. Taivex Therapeutics …

T-1101 Accepted for Online Publication at the 2025 ASCO Annual Meeting, Showcasing Innovative Mechanism and Clinical Potential
Taivex announced that the latest clinical trial data for its novel anticancer drug candidate T-1101 has been accepted for online publication at the 2025 American Society of Clinical Oncology (ASCO) Annual Meeting. As one of the world’s most prestigious oncology conferences, ASCO received over 7,500 abstract submissions this year. The selection of T-1101 underscores the innovation and clinical relevance of …

T-1101 Receives FDA Approval to Advance to Phase II Clinical Trial, Marking a Significant Milestone
Taivex announced that T-1101 has received approval from the U.S. Food and Drug Administration (FDA) to advance to Phase II clinical trials. This trial will further evaluate the safety and efficacy of T-1101 in patients with neuroendocrine tumors (NET), laying a solid foundation for future regulatory submissions. T-1101 is the first-in-class oral small-molecule inhibitor targeting Hec1/Nek2, developed to treat …

T-1101 Receives TFDA Approval for Phase II Clinical Trial, Advancing Development Milestone
Taivex announced that its investigational drug T-1101 has received approval from Taiwan’s Food and Drug Administration (TFDA) to initiate Phase II clinical trials. The study will further evaluate the safety and efficacy of T-1101 in patients with neuroendocrine tumors (NET), supporting the path toward future regulatory filings. T-1101 is a first-in-class oral small-molecule inhibitor targeting Hec1/Nek2, designed to treat …

T-1201 Phase I study design present at 2025 ASCO
The 2025 ASCO Annual Meeting will be held from May 30 to June 3 in Chicago, USA. ASCO (American Society of Clinical Oncology) is the world’s largest and most authoritative clinical oncology meeting, bringing together many of the world’s leading oncology experts, and ASCO is an annual research event that publishes clinical oncology results from around the world. Taivex Therapeutics …

T-1101 Accepted for Online Publication at the 2025 ASCO Annual Meeting, Showcasing Innovative Mechanism and Clinical Potential
Taivex announced that the latest clinical trial data for its novel anticancer drug candidate T-1101 has been accepted for online publication at the 2025 American Society of Clinical Oncology (ASCO) Annual Meeting. As one of the world’s most prestigious oncology conferences, ASCO received over 7,500 abstract submissions this year. The selection of T-1101 underscores the innovation and clinical relevance of …

T-1101 Receives FDA Approval to Advance to Phase II Clinical Trial, Marking a Significant Milestone
Taivex announced that T-1101 has received approval from the U.S. Food and Drug Administration (FDA) to advance to Phase II clinical trials. This trial will further evaluate the safety and efficacy of T-1101 in patients with neuroendocrine tumors (NET), laying a solid foundation for future regulatory submissions. T-1101 is the first-in-class oral small-molecule inhibitor targeting Hec1/Nek2, developed to treat …

Dr. Lun Kelvin Tsou receiving the 14th Tien Te Lee Biomedical Young Scientists Award
Dr. Lun Kelvin Tsou, associate Investigator of IBPR. Dr, Tsou with his team members had development a noval small molecule drug conjugate, DBPR115, that could target a biomarker phosphatidylserine and the deliver the anti-tumor agent to the tumor sites. By increasing the concentration of drug around the tumor, to decrease the side effects. Dr. Tsou was awarded the 14th Tien …

T-1201 get 2017 Taipei Biotech Award_ Technology Transfer Gold Medal Award
Taivex corporate with Institute of Biotechnology and Pharmaceutical Research (IBPR) at National Health Research Institute, developing a first-in-class small molecule drug, T-1201. This drug had received 2016 Technology Achievement Award (Ministry of Economic Affairs), now get 2017 Taipei Biotech Award_ Technology Transfer Gold Medal Award (Taipei City Government). T-1201 is a noval anti-tumor drug deliver system, that with intellectual property …

T-1101 granted the MOEA 2011 Breakthrough Innovation of the Year Award
Taivex corporate with Development Center for Biotechnology (DCB), developed a first-in-class small molecule drug, T-1101. T-1101 is novel oral powder dosage Hec1/Nek2 inhibitor, which block the interaction of Hec1/Nek2 during tumor cell division and lead tumor cell apoptosis and achieve anti-cancer effect. Taivex licensed the lead compound of T-1101, a Hec1/Nek2 inhibitor「Tai-1」from Dr. Wen-Hwa Lee who is Academician, Academia Sinica. …




