Drug intelligence / Profile preview

shr3680 + shr3162

Development stage
Unknown
Lead developer
Hengrui Pharmaceutical
Modality
Small Molecules
Administration
Oral
01

Overview

**SHR3680 + SHR3162** is a combination of two investigational agents developed for oncology indications. **SHR3680** (also known as rezvilutamide) is a novel, orally administered androgen receptor (AR) antagonist. It inhibits AR nuclear translocation, transcriptional activity, and downregulates AR overexpression in prostate cancer cells, effectively suppressing prostate-specific antigen (PSA) secretion without partial agonist activity[1][2][4]. SHR3680 shows lower CNS penetration and seizure risk compared to enzalutamide and is a strong inducer of CYP3A4 and CYP2B6[2]. **SHR3162** is referenced as a companion investigational molecule, but detailed mechanistic and clinical data are not available in the provided sources. The combination likely intends to augment AR pathway inhibition or expand activity within prostate cancer or potentially other hormone-driven malignancies; however, specific details about SHR3162's mechanism are lacking. Primary indication for SHR3680 is metastatic castration-resistant prostate cancer (mCRPC) and metastatic hormone-sensitive prostate cancer (mHSPC)[1][2][3].

Other names
shr3680shr-3680shr 3680shr3162shr-3162shr 3162rezvilutamide
02

Targets

PARP1 (Poly (adp-ribose) polymerase 1)Pol II (RNA polymerase II elongation factors)AR (Adrenergic receptors)

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