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BioWorld - Tuesday, June 16, 2026
Home » Authors » Cormac Sheridan

Articles by Cormac Sheridan

ChronTech's Stock Plummets on HCV Vaccine Phase II Miss

April 3, 2013
By Cormac Sheridan
Shares in ChronTech Pharma AB plunged as much as 40 percent during trading Tuesday on news that ChronVac-C, the company's therapeutic DNA vaccine for treating hepatitis C virus (HCV) infection, failed to attain efficacy in an interim analysis of data from a Phase II trial.
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Themis Plans Trials for Dengue and Chikungunya Vaccines

April 3, 2013
By Cormac Sheridan
Themis Bioscience GmbH is planning to begin clinical trials of viral vaccine candidates to protect against dengue virus and chikungunya virus infections before year-end, following successful preclinical proof of concept studies.
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As Aastrom Falters, ReNeuron Advances Its CLI Cell Therapy

April 3, 2013
By Cormac Sheridan
ReNeuron plc is planning to move its stem cell therapy ReN001 into a Phase I trial in critical limb ischemia (CLI), just as Aastrom Biosciences Inc., an erstwhile leader in the field, is stepping away from the fray.
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Themis Plans Trials for Dengue And Chikungunya Vaccines

April 1, 2013
By Cormac Sheridan
Themis Bioscience GmbH is planning to begin clinical trials of viral vaccine candidates to protect against Dengue virus and Chikungunya virus infections before year-end, following successful preclinical proof of concept studies.
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As Aastrom Falters, ReNeuron Advances Its CLI Cell Therapy

March 28, 2013
By Cormac Sheridan
ReNeuron plc is planning to move its stem cell therapy ReN001 into a Phase I trial in critical limb ischemia (CLI), just as Aastrom Biosciences Inc., an erstwhile leader in the field, is stepping away from the fray.
Read More

Santhera Withdraws Raxone MAA, Plans Resubmission

March 27, 2013
By Cormac Sheridan
With additional data in the offing for its Leber's hereditary optic neuropathy (LHON) drug Raxone (idebenone), Santhera Pharmaceuticals AG has withdrawn its marketing authorization application (MAA) from the European Medicines Agency's (EMA) re-examination process and will instead submit a new file with an expanded patient database.
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SARcode Investors Reap 120% ROI in Sale to Shire

March 26, 2013
By Cormac Sheridan
Underlining its ambitions in ophthalmology, Shire plc is acquiring SARcode Bioscience Inc. for $160 million up front, plus additional, undisclosed milestones based on the clinical, regulatory and commercial progress of its main asset, lifitegrast, which is undergoing a second pivotal Phase III trial in dry eye disease.
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SARcode Investors Reap 120% ROI in Sale to Shire

March 26, 2013
By Cormac Sheridan
Underlining its ambitions in ophthalmology, Shire plc is acquiring SARcode Bioscience Inc. for $160 million up front, plus additional, undisclosed milestones based on the clinical, regulatory and commercial progress of its main asset, lifitegrast, which is undergoing a second pivotal Phase III trial in dry eye disease.
Read More

Santhera Withdraws Raxone MAA, Plans Resubmission

March 25, 2013
By Cormac Sheridan
With additional data in the offing for its Leber's Hereditary Optic Neuropathy (LHON) drug Raxone (idebenone), Santhera Pharmaceuticals AG has withdrawn its marketing authorization application (MAA) from the European Medicines Agency's (EMA) re-examination process and will instead submit a new file with an expanded patient database.
Read More

Safinamide Hits Endpoints in Two Parkinson's Phase III Trials

March 20, 2013
By Cormac Sheridan
Newron Pharmaceuticals SpA and its partner, Zambon SpA, remain on track to file for approval for safinamide as add-on therapy in Parkinson's disease in the fourth quarter, following the release of pivotal Phase III data at the annual meeting of the American Academy of Neurology in San Diego this week.
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