Page contents Key factsDecisionKey facts Active Substance camrelizumab Therapeutic area Neoplasms benign, malignant and unspecified (incl cysts and polyps) Decision number P/0154/2024 PIP number EMEA-003566-PIP01-23 Pharmaceutical form(s) Powder for solution for injection Condition(s) / indication(s) Treatment of hepatocellular carcinoma Route(s) of administration Intravenous use Contact for public enquiries Luzsana Biotechnology EuropeE-mail: regulatoryeu@luzsana.com Tel.: +41 792406071 Decision type W: decision granting a waiver in all age groups for all conditions or indications Decision date 06/05/2024DecisionP/0154/2024: EMA decision of 6 May 2024 on the granting of a product-specific waiver for camreluzimab (EMEA-003566-PIP01-23)Reference Number: EMA/148130/2024 English (EN) (199.8 KB - PDF)First published: 11/06/2025ViewShare this page