A Phase-1 Study Evaluating the Safety, Pharmacology and Preliminary Activity of MM-310 in Patients With Solid Tumors
Latest Information Update: 05 Nov 2021
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At a glance
- Drugs MM 310 (Primary)
- Indications Adenocarcinoma; Carcinoma; Endometrial cancer; Gastric cancer; Non-small cell lung cancer; Oesophageal cancer; Ovarian cancer; Small cell lung cancer; Soft tissue sarcoma; Solid tumours; Squamous cell cancer; Triple negative breast cancer; Urogenital cancer
- Focus Adverse reactions; First in man
- Sponsors Merrimack Pharmaceuticals
- 04 Apr 2019 According to a Merrimack Pharmaceuticals media release, the company expects to initiate a workforce reduction as it closes out clinical activities, reflective of its narrowed preclinical pipeline and in line with prior cost-cutting measures.It also expects to provide an update on these efforts with its first quarter 2019 financial results.
- 04 Apr 2019 According to a Merrimack Pharmaceuticals media release, this study has been terminated as a result of a comprehensive review of available safety data from this phase 1 study. Based on emerging data since the recent amendment of the clinical protocol, the Company has concluded that the study would not be able to reach an optimal therapeutic index for MM-310.
- 04 Apr 2019 Status changed from recruiting to discontinued as the safety update of this phase I study shows that the study unable to reach optimal therapeutic index for MM-310 due to continued observation of cumulative peripheral neuropathy, according to a Merrimack Pharmaceuticals media release.