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Clinical Trial Summary

MM-310 is a liposomal formulation of a docetaxel prodrug that targets the EphA2 receptor on cancer cells. Docetaxel is an approved chemotherapeutic drug.This study is a Phase 1 open-label study of MM-310 in patients with solid tumors. In the first part of the study, MM-310 will be assessed as a monotherapy until a maximum tolerated dose (MTD) is established. After an MTD of MM-310 as a monotherapy is established, an expansion cohort and MM-310 in combination with other therapies will be assessed.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Adenocarcinoma
  • Carcinoma
  • Carcinoma, Non-Small-Cell Lung
  • Carcinoma, Squamous Cell
  • Carcinoma, Transitional Cell
  • Endometrial Carcinoma
  • Endometrial Neoplasms
  • Gastric Carcinoma
  • Head and Neck Neoplasms
  • Lung Neoplasms
  • Non-small Cell Lung Cancer
  • Ovarian Cancer
  • Ovarian Neoplasms
  • Pancreatic Ductal Adenocarcinoma
  • Prostate Adenocarcinoma
  • Prostatic Neoplasms
  • Sarcoma
  • Small Cell Lung Cancer
  • Small Cell Lung Carcinoma
  • Soft Tissue Sarcoma
  • Solid Tumors
  • Squamous Cell Carcinoma of the Head and Neck
  • Stomach Neoplasms
  • Triple Negative Breast Cancer
  • Triple Negative Breast Neoplasms
  • Urothelial Carcinoma

NCT number NCT03076372
Study type Interventional
Source Merrimack Pharmaceuticals
Contact Vasileios Askoxylakis, MD, PhD
Phone 617.441.7492
Email VAskoxylakis@merrimack.com
Status Recruiting
Phase Phase 1
Start date February 22, 2017
Completion date December 2018

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