Latest Hotspot

FDA Approves KaliVir Immunotherapeutics' VET3-TGI for Solid Tumor Immunotherapy

5 July 2024
3 min read

KaliVir Immunotherapeutics, Inc., a biotechnology firm focused on creating advanced, multi-mechanistic oncolytic viral immunotherapy programs, has reported that the FDA has approved the Investigational New Drug application for the STEALTH-001 trial of VET3-TGI in patients with terminal, advanced solid tumors.

👇Discover comprehensive information about this drug, from its R&D status, core patents, clinical trials to approval status in global countries, by simply clicking on the image below. Dive deep into our drug database now.

图形用户界面, 文本, 应用程序, 电子邮件

描述已自动生成

VET3-TGI represents an innovative form of oncolytic immunotherapy, designed to selectively target and destroy tumor cells while also enhancing anti-cancer immune responses through the expression of interleukin-12 and a TGFbeta inhibitor. Nonclinical studies have demonstrated its ability to effectively kill cancer cells while promoting immune system activation.

The Phase 1/1b clinical trial is set to investigate the safety and effectiveness of VET3-TGI, administered either via intravenous infusion or directly into the tumor, in patients suffering from advanced, inoperable solid tumors. This study will examine VET3-TGI as a standalone treatment as well as in conjunction with checkpoint inhibitor therapy.

"The launch of this Phase 1/1b clinical trial signifies a crucial step in our mission to revolutionize cancer therapy using oncolytic virus approaches, particularly for advanced, unmanageable, or metastatic solid tumors," commented Helena Chaye, Ph.D., CEO of KaliVir Immunotherapeutics.

"This is our second clinical trial initiation under the VET platform, following the 2023 progress of ASP1012, which is exclusively licensed to Astellas. We are dedicated to expanding the possibilities of cancer treatment, developing safer and more effective therapeutic options that could potentially reshape the oncology treatment landscape," added Helena Chaye.

👇Explore the latest research progress on drug-related developments, indications, therapeutic organizations, clinical trials, results, and patents by clicking on the targeted picture link below. Unfold a world of comprehensive information on this target in just a click!

图形用户界面, 应用程序, 电子邮件

描述已自动生成

According to the data provided by the Synapse Database, As of July 5, 2024, there are 1 investigational drug for the CXCR3, IL-12, and TGF-β targets, including 9 indications, 1 R&D institution involved, with related clinical trial reaching 1, and as many as 412 patents.

VET3-TGI is an oncolytic virus that targets CXCR3, IL-12, and TGF-β. VET3-TGI is an oncolytic virus with a broad range of therapeutic areas and active indications, particularly focusing on various types of cancer. 

How to obtain the latest research advancements in the field of biopharmaceuticals?

In the Synapse database, you can keep abreast of the latest research and development advances in drugs, targets, indications, organizations, etc., anywhere and anytime, on a daily or weekly basis. Click on the image below to embark on a brand new journey of drug discovery!

图形用户界面, 文本, 应用程序, 聊天或短信

描述已自动生成

Is Somapacitan approved by the FDA?
Drug Insights
3 min read
Is Somapacitan approved by the FDA?
5 July 2024
Approved on August 28, 2020, somapacitan (Sogroya) offers a convenient once-weekly injection, improving adherence and quality of life for patients.
Read →
Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Jul 5
Pharma Frontiers
10 min read
Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Jul 5
5 July 2024
Jul 5th latest updates in the global new drug development field, including progress in new drug research and development, transaction information, and partnership developments.
Read →
Is Clascoterone approved by the FDA?
Drug Insights
3 min read
Is Clascoterone approved by the FDA?
5 July 2024
Approved on August 26, 2020, clascoterone (Winlevi) offers a novel mechanism of action by inhibiting androgen receptors in the skin, reducing oil production and inflammation associated with acne.
Read →
Idorsia's JERAYGO: Europe's First and Only ERA Approved for Resistant Hypertension
Latest Hotspot
3 min read
Idorsia's JERAYGO: Europe's First and Only ERA Approved for Resistant Hypertension
5 July 2024
Idorsia’s JERAYGO (aprocitentan) approved in Europe as the first and only ERA for resistant hypertension treatment.
Read →
Get started for free today!
Accelerate Strategic R&D decision making with Synapse, PatSnap’s AI-powered Connected Innovation Intelligence Platform Built for Life Sciences Professionals.
Start your data trial now!
Synapse data is also accessible to external entities via APIs or data packages. Empower better decisions with the latest in pharmaceutical intelligence.