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propranolol + sintilimab + chemotherapy
- Development stage
- Unknown
- Lead developer
- The Second Xiangya Hospital
- Modality
- Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
- Administration
- Oral, Intravenous
01
Overview
This investigational combination therapy is being evaluated as a first-line treatment for advanced non-small cell lung cancer (NSCLC) that is negative for EGFR, ALK, and ROS1 driver mutations. The regimen consists of **propranolol hydrochloride**, a non-selective beta-adrenergic receptor antagonist; **sintilimab**, a recombinant humanized IgG4 monoclonal antibody targeting the programmed cell death protein 1 (PD-1) receptor; and standard **platinum-based chemotherapy** (typically cisplatin or carboplatin combined with pemetrexed, paclitaxel, or gemcitabine). Propranolol is included to potentially modulate the tumor microenvironment and augment immune cell responses, thereby enhancing the efficacy of the immune checkpoint inhibitor sintilimab. The combination is currently under investigation in a Phase I clinical trial (BRIO) sponsored by the Second Xiangya Hospital of Central South University.
- Other names
- propranolol hydrochloride in combination with sintilimab and platinum-based chemotherapy
02
Targets
DNAADRB2 (β2)PDCD1 (Programmed cell death protein 1 receptor)ADRB1 (β1)
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