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Molecular Targeting Technologies, Inc., Thomas Jefferson University and North China Pharmaceutical Co., Ltd Announced the Chinese Approval for a Rabies Drug

WEST CHESTER, Pa. (BUSINESS WIRE) Jan 26, 2022 ....

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Molecular Targeting Technologies, Inc. and University of Antwerp Begin First-in-Human Study of TDURA Diagnostic for Early Detection of Response to Colon Cancer Therapy

Published: May 11, 2021

WEST CHESTER, Pa. (BUSINESS WIRE) Molecular Targeting Technologies, Inc. (MTTI) and University of Antwerp today announced the approval of a Clinical Trial Application by the European Federal Agency for Medicines and Health Products (FAMHP) (equivalent to a US IND). The clinical study will evaluate the safety, dosimetry and treatment response of TDURA (
99mTc-Duramycin), in patients with advanced colorectal cancer (CRC) .
Colorectal cancer is the third most commonly diagnosed malignancy in the world and the second leading cause of cancer death in the United States. While a range of novel active agents has improved the prognosis of patients with colorectal cancer, 50% of advanced colorectal cancer patients die from metastatic disease. ....

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Molecular Targeting Technologies, Inc. Announces New PET Imaging Agent

Molecular Targeting Technologies, Inc. Announces New PET Imaging Agent
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Molecular Targeting Technologies, Inc. Announces a New PET Imaging Agent for Rapid Monitoring Tumor Response to Therapy

Molecular Targeting Technologies, Inc. Announces a New PET Imaging Agent for Rapid Monitoring Tumor Response to Therapy
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FDA Approves Investigational New Drug (IND) for Neuroendocrine Tumors from Molecular Targeting Technologies, Inc.

Press release content from Business Wire. The AP news staff was not involved in its creation.
FDA Approves Investigational New Drug (IND) for Neuroendocrine Tumors from Molecular Targeting Technologies, Inc.
March 2, 2021 GMT
WEST CHESTER, Pa. (BUSINESS WIRE) Mar 2, 2021
Molecular Targeting Technologies, Inc. (MTTI), a clinical stage radiopharmaceutical therapy company focused on therapies for rare diseases, announced today the approval of an Investigational New Drug (IND) application by the U.S. Food and Drug Administration (FDA). It enables a Phase I clinical study of the Safety and Dosimetry of its lead product, EBTATE ( 177 Lu-DOTA-EB-TATE), in patients with neuroendocrine tumors (NET). ....

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