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RESEARCH TRIANGLE PARK, NC – JANUARY 27, 2015 – Envisia Therapeutics today announced that it has initiated a phase 2a clinical trial to investigate the safety and tolerability of its lead product, ENV515, in patients with glaucoma. ENV515 is a proprietary, fully biodegradable PRINT® (Particle Replication In Non-Wetting Templates) particle formulation of a prostaglandin analog, travoprost, with the potential for sustained intraocular pressure (IOP) reduction over as many as six months. ENV515 offers the potential to significantly address the poor compliance that exists among glaucoma patients today to limit disease progression and vision loss.

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HAYWARD, Calif. and SHANGHAI, Feb. 25, 2015 /PRNewswire/ -- MicuRx Pharmaceuticals, Inc., a privately-held biopharmaceutical company developing next-generation antibiotics, today announced that it has received the approval from the U.S. Food and Drug Administration (FDA) to initiate Phase 2 clinical study in the United States for its lead drug candidate MRX-I. MRX-I, which demonstrated an enhanced safety profile over the market-leading comparator in Phase 1 studies, is an oral oxazolidinone antibiotic designed to treat infections caused by Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE).

RESEARCH TRIANGLE PARK, NC – OCTOBER 6, 2015 – Envisia Therapeutics, a clinical-stage biotechnology company focused on the development of novel extended-release therapies in ophthalmology, today reported results from its first clinical trial of the Company’s lead product candidate, ENV515 (travoprost XR). In this phase 2a trial, ENV515 achieved its primary efficacy endpoint by demonstrating a statistically significant and clinically meaningful reduction in intraocular pressure (IOP) with results comparable to topical once-daily TRAVATAN Z® (travoprost ophthalmic solution). ENV515 is engineered as a proprietary, fully biodegradable PRINT® (Particle Replication In Non-Wetting Templates) travoprost formulation that could offer sustained reduction in IOP for more than six months after a single dose.

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There are a number of steps regarding submission and examination that the Principal supervisor should be aware of when Thesis Submission Forms – University College Dublin Information on UCD exams, exam key dates, exam timetables, exam tips, exam past papers, mcqs, exam arrangements, exam temporary support, exam Graduate Research Thesis Registration Extension Form – University UNIVERSITY COLLEGE DUBLIN Students should ensure that they read section 4 (Pre-thesis submission: Extension) in the Policy on to the School Office as soon as possible and normally in advance of the thesis submission deadline.

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How to submit – Research Repository UCDUniversity College Dublin How to submit papers to Research Repository UCD At this time we are not able to accept theses, Powerpoint presentation slides (although if you deem these Page 1 of 4 Recommendations for the Presentation of Theses University College Dublin.

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Policy on Theses in Graduate Taught Programmes – SISWeb 23 Apr 2010 www.ucd.ie/registry/academicsecretariat Ensure that the process of thesis submission and examination is conducted in a transparent,.

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