Drug intelligence / Profile preview

bortezomib + dexamethasone + doxorubicin + acetyl-l-carnitine

Development stage
Unknown
Lead developer
Takeda
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, DNA Intercalators/Alkylators → Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Intravenous, Subcutaneous, Oral
01

Overview

This is a four-drug combination therapy consisting of bortezomib, dexamethasone, doxorubicin, and acetyl-l-carnitine (ALCAR), primarily investigated for the treatment of relapsed or refractory multiple myeloma. Bortezomib is a reversible inhibitor of the 26S proteasome, disrupting protein degradation and inducing apoptosis in malignant cells. Dexamethasone is a synthetic glucocorticoid with anti-inflammatory and immunosuppressive effects. Doxorubicin is an anthracycline antibiotic that intercalates DNA and inhibits topoisomerase II, leading to cytotoxicity in rapidly dividing cells. Acetyl-l-carnitine is included as a neuroprotective agent to reduce the incidence and severity of peripheral neuropathy associated with bortezomib-based regimens[1][4]. This combination has demonstrated high response rates even in heavily pretreated multiple myeloma patients[1].

Brand names
Velcade (bortezomib)Adriamycin (doxorubicin)Decadron (dexamethasone)
Other names
PAD regimen plus acetyl-l-carnitineBDD-A regimen
02

Targets

GR (Glucocorticoid receptor)TOP2A (DNA topoisomerase II)PSMB5 (Proteasome subunit beta Type-5)

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