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151. The US FDA authorises new oral treatment Mavenclad for multiple sclerosis

152. The US FDA authorises new oral treatment Mavenclad for multiple sclerosis

153. Mavenclad (Cladribine Tablets) Receives First Approval in Latin America

154. Mavenclad (Cladribine Tablets) Receives First Approval in Latin America Feb 26, 2018

155. Mavenclad (Cladribine Tablets) Receives First Approval in Latin America

156. 2017 Mavenclad Drug Analysis: A Small Molecule that Suppresses the Immune System by Selectively Targeting Lymphocytes - ResearchAndMarkets.com

157. 2017 Mavenclad Drug Analysis: A Small Molecule that Suppresses the Immune System by Selectively Targeting Lymphocytes - ResearchAndMarkets.com

158. 2017 Mavenclad Drug Analysis: A Small Molecule that Suppresses the Immune System by Selectively Targeting Lymphocytes

159. Supply Of Cladribine (mavenclad) (united Kingdom-edinburgh: Pharmaceutical Productsnd)

160. Supply Of Cladribine (mavenclad)

161. Merck's Mavenclad Approved for Relapsing-Remitting Multiple Sclerosis in Canada

162. Merck's Mavenclad (Cladribine Tablets) Approved for Relapsing-Remitting Multiple Sclerosis in Canada

163. Merck's Mavenclad (Cladribine Tablets) Approved for Relapsing-Remitting Multiple Sclerosis in Canada

164. Merck's Mavenclad (Cladribine Tablets) Approved for Relapsing-Remitting Multiple Sclerosis in Canada

166. NICE Recommends Mavenclad (Cladribine Tablets) for Highly Active Multiple Sclerosis

167. NICE Recommends Mavenclad (Cladribine Tablets) for Highly Active Multiple Sclerosis

168. New Data at ECTRIMS Highlight Positive Benefit-Risk Profile of Mavenclad in Relapsing Multiple Sclerosis

169. Merck to Present New Data on MS Portfolio: Rebif, Mavenclad, and Evobrutinib at ECTRIMS 2017

170. Register of Commission documents:Formal results of voting on: MAVENCLAD - Authorisation - CT Document date: 2017-07-19 COM-AC_DR(2017)V052822-01(VOT) Comitology - Right of scrutiny

171. European Commission Grants Approval for Mavenclad (Cladribine Tablets)

172. Merck - European Commission Grants Approval for Mavenclad

173. European Commission Grants Approval for Mavenclad (Cladribine Tablets)

174. Cladribine (Mavenclad) for MS Approved in Europe

175. Merck passes European Commission's approval for Mavenclad for treating highly active relapsing multiple sclerosis in the EU

176. Argentinian Regulatory Agency Grants Approval for Mavenclad (Cladribine Tablets) for Treatment of Relapsing MS

177. Merck passes Health Canada's approval for MAVENCLAD (Cladribine Tablets) to treat relapsing-remitting multiple sclerosis

178. Merck passes Health Canada's approval for MAVENCLAD (Cladribine Tablets) to treat relapsing-remitting multiple sclerosis

179. European Commission grants marketing authorisation to Merck's MAVENCLAD

180. European Commission grants marketing authorisation to Merck's MAVENCLAD

181. Merck's Mavenclad gets EU approval as a treatment for MS

182. Merck's Mavenclad gets EU approval as a treatment for MS

183. Merck passes European Commission's approval for Mavenclad for treating highly active relapsing multiple sclerosis in the EU

184. Merck passes European Commission's approval for Mavenclad for treating highly active relapsing multiple sclerosis in the EU

185. Pharmaceutical Times - NICE backs Merck's Mavenclad for MS - 10/11/2017

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