Glembatumumab vedotin - Celldex Therapeutics Inc

Drug Profile

Glembatumumab vedotin - Celldex Therapeutics Inc

Alternative Names: CDX-011; CR 011 ADC; CR 011-vcMMAE; CR011-vcMMAE immunotoxin; Glemba; Glembatumumab; GV

Latest Information Update: 14 Nov 2017

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At a glance

  • Originator CuraGen Corporation
  • Developer Celldex Therapeutics Inc; National Cancer Institute (USA)
  • Class Antineoplastics; Auristatins; Drug conjugates; Immunotoxins; Monoclonal antibodies
  • Mechanism of Action Apoptosis stimulants; Mitosis inhibitors; Tubulin inhibitors; Tubulin polymerisation inhibitors
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    No
  • New Molecular Entity Yes
  • Available For Licensing Yes

Highest Development Phases

  • Phase II Breast cancer; Malignant melanoma; Osteosarcoma; Uveal melanoma
  • Phase I/II Squamous cell cancer
  • Discontinued Brain cancer

Most Recent Events

  • 07 Nov 2017 Efficacy data from a phase II trial in Uveal melanoma released by Celldex
  • 06 Nov 2017 National Cancer Institute plans a phase Ib/II trial for Solid tumours (Late-stage disease, Metastatic disease, Inoperable/Unresectable, Combination therapy, Second-line therapy or greater) in June 2018 (NCT03326258)
  • 23 Aug 2017 Celldex Therapeutics completes enrolment in the phase IIb METRIC trial for Breast cancer (Late-stage disease, Metastatic disease, Second-line therapy or greater) in USA, Australia, Belgium, Canada, Germany, Italy, France, Spain and United Kingdom (NCT01997333)
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