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BioWorld - Thursday, April 30, 2026
Breaking News: Read BioWorld's AACR 2026 coverageBreaking News: Best of BioWorld: Q1
Home » Topics » BioWorld, Clinical

BioWorld, Clinical
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Dimas Covas, director, Butantan Institute
Approval likely even with new data

Brazil says Sinovac COVID-19 vaccine is about 50% effective, much lower than earlier results

Jan. 13, 2021
By Sergio Held
CAJICA, Colombia – Authorities in Brazil released new efficacy data for Sinovac Biotech Ltd.'s COVID-19 vaccine Coronavac that surprised on the downside, suggesting the vaccine could be much less effective than initially indicated for preventing symptomatic infections.
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In the clinic for Jan. 13, 2021

Jan. 13, 2021
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Adastra, Arcutis, Celltrion, Cytokinetics, Fosun, Gensight, Jounce, Kintara, Leo, Philogen, Regeneron, Rockwell, Sanofi, Sorrento, Synairgen.
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In the clinic for Jan. 12, 2021

Jan. 12, 2021
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Ascletis, Blue Earth, Bone Therapeutics, Caladrius, Cellectar, Clearside, Clovis, Gannex, GSK, GT, Helsinn, Lipocine, Merus, Mesoblast, Ox2, Resverlogix, Rezolute, Roche, Taiho, Terns, Vir, Vitalis.
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Brain teaser

Lilly shares leap on phase II Alzheimer's disease data

Jan. 11, 2021
By Michael Fitzhugh
Shares of Eli Lilly and Co. (NYSE:LLY) leapt 11.7% to $185.94, their second biggest gain since 2010, after a phase II trial showed its beta-amyloid-targeting monoclonal antibody, donanemab, appeared to slow by 32% decline in a composite measure of cognition and daily function in patients with early symptomatic Alzheimer’s disease vs. placebo.
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Mosaico team in Mexico City

First-ever phase III trials of HIV vaccine in Latin America

Jan. 11, 2021
By Sergio Held
CAJICA, Colombia – A phase III trial for an HIV vaccine developed Janssen Vaccines & Prevention BV is finally moving forward in Latin America and elsewhere in the world after a delay of more than a year caused by slow regulatory progress and worsened by a string of COVID-19 lockdowns.
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Ascentage’s New Year’s resolution includes getting its first candidate to market

Jan. 11, 2021
By Gina Lee
HONG KONG – Tapping into synergies it sees between the U.S. and Chinese biotech industries, Suzhou, China-based Ascentage Pharma Group Corp. Ltd. is aiming to get its most advanced candidate, HQP-1351 (olverembatinib dimesylate) to market this year for patients with TKI-resistant chronic myeloid leukemia.
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In the clinic for Jan. 11, 2021

Jan. 11, 2021
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Adverum, Aptevo, Aslan, Biomarin, Can-Fite, Cara, Celon, Codagenix, Dalcor, Dr. Reddy's, Edesa, Inflarx, Jupiter Orphan, Kintor, Lilly, Mediwound, Mesoblast, Neurorx, Oric, Redhill, Relief, Ultimovacs.
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Doctor examining child in wheelchair

Sarepta DMD phase II hangs in ‘balance’ as disparity in North Star leads astray

Jan. 8, 2021
By Randy Osborne
Sarepta Therapeutics Inc.’s miss on a key phase II ambulatory endpoint in its Duchenne muscular dystrophy (DMD) trial may have been caused by a dramatic disparity in functional ability at baseline among older vs. younger patients afflicted with the progressively worsening disorder. In any case, Wall Street had knives out, carving 51% of the value away from shares (NASDAQ:SRPT) of the Cambridge, Mass.-based firm, which closed at $82.29, a loss of $86.66, or 51%.
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In the clinic for Jan. 8, 2021

Jan. 8, 2021
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Biogen, Can-Fite, Denovo, Dynavax, Dermbiont, Felix, Gradalis, Graybug, Inmed, Immutep, Leading Bio, Northsea, Oncosec, Prilenia, Proqr, Remd, Rhovac, Sarepta, Translate Bio, Ultragenyx.
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Silhouette of person walking with a cane

Chariot to admire: Alnylam finds place in sun with Helios-A phase III

Jan. 7, 2021
By Randy Osborne
Alnylam Pharmaceuticals Inc. said the 164-patient Helios-A phase III study with next-generation RNAi drug vutrisiran hit its primary endpoint as well as both secondary goals in the treatment of hereditary transthyretin-mediated amyloidosis with polyneuropathy. The primary endpoint was change from baseline in the modified Neuropathy Impairment Score at nine months as compared to historical placebo data from the Apollo phase III study of Alnylam’s Onpattro, cleared by the FDA for ATTR polyneuropathy in August 2018.
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