Glembatumumab vedotin

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Glembatumumab vedotin
Monoclonal antibody
Type Whole antibody
Source Human
Target GPNMB
Clinical data
Legal status
  • Investigational
Identifiers
CAS Number 1020264-78-1 N (glembatumumab)
ATC code none
KEGG D09912 N
 NYesY (what is this?)  (verify)

Glembatumumab vedotin (also known as CDX-011 and CR011-vcMMAE) is an antibody-drug conjugate (ADC) that targets cancer cells expressing transmembrane glycoprotein NMB (GPNMB).

In May 2010, the U.S FDA granted Fast Track designation to CDX-011 for the treatment of advanced, refractory or resistant GPNMB-expressing breast cancer.[1]

Structure and mechanism

The fully human IgG2 monoclonal antibody glembatumumab (CR011) is linked to monomethyl auristatin E (MMAE).

It uses a valine-citrulline enzyme-cleavable linker.[2]

The linkage is stable in the bloodstream. The antibody binds to GPNMB on the cancer cells, the ADC is internalised, the linkage is broken and MMAE is released to kill the cell.[3]

In preclinical studies glembatumumab vedotin was capable of killing GPNMB expressing melanoma and breast cancer cells in vitro[4][5] and inducing partial or complete regression of GPNMB-expressing tumors in mouse models.[3][5][6]

Clinical trials

In September 2010 a Phase 2b clinical study started of glembatumumab vedotin in 120 patients with GPNMB-expressing breast cancer including those with triple negative breast cancer.

As of June 2011, Phase I/II clinical trials of glembatumumab vedotin for the treatment of advanced melanoma[7] and breast cancer[8] have been completed but no official study result was posted. Preliminary results from these trials have shown that glembatumumab vedotin has some clinical activity (promotes tumor shrinkage) in both cancer types.[9] Patients whose tumors express GPNMB respond better to glembatumumab and have longer progression-free survival than those whose tumors do not express GPNMB.[10][11]

An accelerated approval Phase II clinical trial investigating glembatumumab vedotin versus capecitabine (2:1 with crossover allowed) has begun enrolling 300 patients with GPNMB-expressing metastatic triple negative breast cancer. Patients who have progressed after receiving anthracyclines and taxanes are eligible.[12]

References

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  9. Celldex: Scientific Articles
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