Drug intelligence / Profile preview

chidamide + cyclophosphamide + prednisone + thalidomide

Development stage
Unknown
Lead developer
Jiangsu Provincial People's Hospital
Modality
Small Molecules
Administration
Oral
01

Overview

C-CPT, commonly termed the **CPCT regimen**, is an investigational all-oral co-administration regimen for fragile patients with relapsed or refractory peripheral T-cell lymphoma who cannot tolerate standard chemotherapy. It combines the selective histone deacetylase inhibitor chidamide with low-dose metronomic cyclophosphamide, prednisone, and thalidomide, followed by chidamide maintenance after induction. In the registered multicenter Phase II study NCT02879526, the regimen used chidamide 30 mg twice weekly, cyclophosphamide 50 mg daily, prednisone 20 mg daily, and thalidomide 100 mg daily. ([clinicaltrials.gov](https://clinicaltrials.gov/study/NCT02879526))

Other names
C-CPTC-PCTCPCTchidamide + cyclophosphamide + prednisone + thalidomidechidamide + prednisone + cyclophosphamide + thalidomide
02

Targets

CRBN (Cereblon)DNAGR (Glucocorticoid receptor)HDAC1 (Histone Deacetylase 1)HDAC10 (Histone Deacetylase 10)HDAC2 (Histone deacetylase 2)HDAC3 (Histone Deacetylase 3)

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