The data from the third and final part of Verona’s Phase I/IIa trial of RPL554 is unequivocally positive. Following previously reported data in healthy volunteers, today’s data in COPD patients demonstrates both reproducibility of the excellent safety & tolerability profile of the new formulation and strong indications of efficacy, with a clinically meaningful improvement in lung function (as measured by FEV1). We upgrade our intrinsic value from 7p to 9p/share and see further upside potential.

29 Sep 2015
RPL554 meets trial endpoints in COPD patients

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RPL554 meets trial endpoints in COPD patients
Verona Pharma plc Sponsored ADR (VRNA:NAS) | 0 0 0.0%
- Published:
29 Sep 2015 -
Author:
Singer CM Team -
Pages:
4 -
The data from the third and final part of Verona’s Phase I/IIa trial of RPL554 is unequivocally positive. Following previously reported data in healthy volunteers, today’s data in COPD patients demonstrates both reproducibility of the excellent safety & tolerability profile of the new formulation and strong indications of efficacy, with a clinically meaningful improvement in lung function (as measured by FEV1). We upgrade our intrinsic value from 7p to 9p/share and see further upside potential.