Crucell Rabies Monoclonal Antibody Combination: Positive Results Philippines Phase II Study Presented at RITA Conference
In June 2009, Crucell announced the results of the Phase II Philippines study in healthy adolescents and children, which showed that the antibody combination was safe and well tolerated. Neutralizing activity levels in subjects given the antibody product were similar to those in subjects given human rabies immunoglobulin (HRIG), the current standard for inducing immediate, passive immunity. All study participants reached adequate immunity levels. This study in a paediatric population, performed at the Research Institute for Tropical Medicine under the leadership of Dr Quiambao, further broadens the potential patient population for Crucell's rabies monoclonal antibody combination.
"We continue to push this program forward in order to bring a high quality rabies treatment to the market as soon as possible. Plans to start the third phase II clinical study are progressing well after recent approval received from the Drug Controller General of India." said Ronald Brus, CEO Crucell. "The market for Crucell's rabies monoclonal antibody combination is estimated to be significant with peak sales expected to exceed $300 million."
This third phase II study will be carried out at Lotus Laboratories in Bangalore, India and is planned to start within the next six months. The rationale for this study is to collect safety and neutralizing activity data of the CL184 antibody in combination with the vaccine in a simulated rabies post-exposure prophylaxis setting to be used in Phase III.
Crucell's monoclonal antibody combination against rabies is being developed in close collaboration with Sanofi Pasteur using Crucell's PER.C6® manufacturing technology. This antibody combination is designed to be used in combination with a rabies vaccine for post-exposure prophylaxis against this fatal disease.
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