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BioWorld - Monday, February 23, 2026
Home » Topics » Clinical

Clinical
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Kodiak moment spoiled, shares bearish as AMD study fails to Dazzle

Feb. 23, 2022
By Randy Osborne
Kodiak Sciences Inc. shares (NASDAQ:KOD) closed at $9.86, down $40.49, or 80.42% after the firm unveiled top-line data from its randomized, double-masked, active comparator-controlled phase IIb/III trial testing KSI-301, an antibody biopolymer conjugate, in treatment-naïve subjects with wet age-related macular degeneration (AMD).
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Coronavirus and antibodies

Sanofi-GSK poised to seek approval for new COVID-19 vaccine

Feb. 23, 2022
By Lee Landenberger
In the quest for regulatory approval for their COVID-19 vaccine, Sanofi SA and Glaxosmithkline plc (GSK) said they plan to submit their phase III and booster efficacy study data showing it induced a significant increase in neutralizing antibodies after a primary series of mRNA or adenovirus vaccines.
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Man wearing Parasym device in ear

The beat goes on: Bioelectronics reduce heart failure symptoms, afib risk and tinnitus

Feb. 22, 2022
By Annette Boyle
Several recent studies highlight the rapidly expanding applications for neuromodulation using bioelectronic devices. A pair of articles in the Journal of the American Heart Association and Journal of the American College of Cardiology focused on the benefits to patients with heart failure and those at risk of post-operative atrial fibrillation, respectively. A study published in Brain Stimulation found that 85% of tinnitus patients experienced resolution of their symptoms when using a neuromodulation device.
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Wall Street high on LSD1; mid-stage, early trips underway

Feb. 22, 2022
By Randy Osborne
Jubilant Therapeutics Inc. started 2022 with an IND clearance for JBI-802, its oral, selective dual inhibitor of lysine-specific demethylase 1 (LSD1) and HDAC6, setting up a year that could be important for LSD1 in the hands of others as well.
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Synairgen shares smashed after phase III trial of inhaled COVID therapy fails

Feb. 22, 2022
By Richard Staines
Shares in Synairgen plc have cratered after a phase III trial of its inhaled COVID-19 therapy SNG-001 failed to produce conclusive results, with the company blaming improvements in standard care for the disappointing findings in patients hospitalized with the disease. The Southampton, U.K.-based biotech’s shares (LSE:SNG) touched lows of 10 pence, down 94%, and stabilized around 85% below their previous closing price of £25.36 after the announcement on Monday.
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Livzon’s COVID-19 vaccine as a booster shot shows efficacy against omicron variant

Feb. 22, 2022
By Doris Yu
Livzon Pharmaceutical Group Inc.’s key interim data from the phase III trials of its recombinant SARS-CoV-2 fusion protein vaccine, V-01, has shown efficacy against the omicron variant. The phase III trial aims to evaluate the efficacy, safety and immunogenicity of V-01 as a booster in adults older than 18 after they have received two doses of inactivated vaccines.
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Thyroid anatomy

Ascendis rising in HPT, Natpara comparator off base?

Feb. 18, 2022
By Randy Osborne
Phase III data are due any day from Ascendis Pharma A/S, and Wall Street’s thoughts have turned to hypoparathyroidism (HPT), an indication fraught with questions in recent years.
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Livzon’s COVID-19 vaccine as a booster shot shows efficacy against omicron variant

Feb. 18, 2022
By Doris Yu
Livzon Pharmaceutical Group Inc.’s key interim data from the phase III trials of its recombinant SARS-CoV-2 fusion protein vaccine, V-01, has shown efficacy against the omicron variant. The phase III trial aims to evaluate the efficacy, safety and immunogenicity of V-01 as a booster in adults older than 18 after they have received two doses of inactivated vaccines.
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GSK pauses late-stage trial of potential blockbuster RSV vaccine

Feb. 18, 2022
By Richard Staines
Glaxosmithkline plc has voluntarily paused a late-stage trial of its potential respiratory syncytial virus (RSV) maternal vaccine candidate in pregnant women following a safety warning. In a brief statement, the London-based firm said it also paused recruitment in two other trials investigating the drug in pregnant women.
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Marker’s phase II data and pipeline expansion prompt market wobble

Feb. 17, 2022
By Lee Landenberger
Marker Therapeutics Inc.’s update from the safety lead-in stage of its phase II study of MT-401 in treating post-transplant acute myeloid leukemia saw response in one of the six participants. The results from the study of the multitumor-associated antigen-specific T-cell product also known as zelenoleucel saw firms such as Oppenheimer cut its target price for Marker to $5 from $8 and Piper Sandler to cut its target price from $5.50 to $4.
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