Drug intelligence / Profile preview

panobinostat + docetaxel + prednisone

Development stage
Phase 1
Lead developer
Novartis
Modality
Small Molecules
Administration
Oral, Intravenous
01

Overview

Panobinostat + docetaxel + prednisone is an experimental combination therapy evaluated for the treatment of metastatic castration-resistant prostate cancer (mCRPC). **Panobinostat** is a pan-histone deacetylase (HDAC) inhibitor that induces cell cycle arrest and apoptosis by modulating gene expression. **Docetaxel** is a taxane-class cytotoxic chemotherapeutic that inhibits microtubule depolymerization, causing cell-cycle arrest at the G2/M phase. **Prednisone** is a synthetic glucocorticoid used for its anti-inflammatory and immunosuppressive properties, and also commonly paired with docetaxel in mCRPC to reduce some side effects and possibly enhance efficacy. This combination was tested in phase I trials to determine safety and early indications of activity in castration-resistant prostate cancer, showing some preliminary evidence of PSA reduction and feasibility for further study[1][3][6].

Brand names
Farydak (for panobinostat)
02

Targets

GR (Glucocorticoid receptor)HDAC1 (Histone Deacetylase 1)HDAC10 (Histone Deacetylase 10)HDAC11 (Histone Deacetylase 11)HDAC2 (Histone deacetylase 2)HDAC3 (Histone Deacetylase 3)HDAC4HDAC5 (Histone deacetylase 5)HDAC6 (Histone deacetylase 6)HDAC7HDAC8 (Histone Deacetylase 8)HDAC9TUBB (Tubulin (alpha and beta subunits))

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