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Synergies between Regulatory and Health Technology Assessments – ISPOR 19th Annual European Congress – 29 Oct-2 Nov 2016, Vienna, Austria

The International Society for Pharmacoeconomics and Outcomes Research (ISPOR) opened last Monday its 19th Annual European Congress in Vienna, Austria with a plenary session entitled What Synergies Could Be Created Between Regulatory and Health Technology Assessments?The plenary discussion was moderated by

ESMO 2016 – Congress Highlights

Kinesys Oncology: ESMO Congress, Copenhagen, 7-11 October 2016 Update on Lung Cancers, plus selected highlights in other tumours  Lung Cancer: http://emarketing.atalanta.uk.com/t/y-F1A2BEE45251C66C RCC, Prostate, SCLC, Gastro-Oesophageal Cancers: http://emarketing.atalanta.uk.com/t/y-0F73DC93CC39BBDA NSCLC AstraZeneca: Selumetinib misses primary endpoint. Durvalumab: 80%, 6-month survival in Phase I / II

Haemato-Oncology Orphan Drugs

Why is the World of Orphan Haemato-Oncology Agents Changing?As an increasing number of targeted oncology and haematology products are getting approved by EMA and FDA, the orphan space is becoming more and more crowded in these therapeutic areas.Patients with a

Orphan Designation for SGX301 in CTCL

Kinesys Consulting Ltd is pleased to announce that the European Commission, acting on the positive recommendation from the European Medicines Agency (EMA) Committee for Orphan Medicinal Products (COMP), has granted orphan drug designation to SGX301(synthetic hypericin) for the treatment of

Biosimilars Kinesys USA Nov 2015

Kinesys' CEO Gerry McGettigan will present on Regulatory & Commercial aspects of Biosimilars at the SMi Conference on 16 November 2015, Renaissance Woodbridge Hotel, Iselin, New Jersey. On 17 November, Gerry and Kinesys' Product Development Expert Graeme Deuchar will hold an interactive workshop