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BioWorld - Thursday, December 25, 2025
Home » Authors » Randy Osborne

Articles by Randy Osborne

Illustration of neurons with Lewy bodies

Enhanced Cognition: Lewy body dementia phase II pumps stock

Dec. 18, 2024
By Randy Osborne
Investors will get more details during the International Lewy Body Dementia Conference in Amsterdam late next month, but Wall Street is already buzzing about Cognition Therapeutics Inc.’s data from the phase II study with CT-1812 in dementia with Lewy bodies.
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Happier new year? Tenaya to raise HCM gene therapy dose

Dec. 17, 2024
By Randy Osborne
Wall Street must wait until 2025 for data from the higher-dose cohort in Tenaya Therapeutics Inc.’s phase Ib/II study with gene therapy TN-201 for MYBPC3-linked hypertrophic cardiomyopathy (HCM), but shares (NASDAQ:TNYA) closed Dec. 17 at $1.41, down $1.47, or 51%, after results from the first cohort rolled out.
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Ovarian cancer illustration

Drug duo to Repare lack in gyno cancers? Phase I shows promise

Dec. 13, 2024
By Randy Osborne
Wall Street wasn’t jumping up and down about Repare Therapeutics Inc.’s early data in gynecological cancers, though the findings look positive and the company has big plans for the combo therapy.
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Lungs

Trial’d on for size, Trevi’s Haduvio fits nice in IPF cough

Dec. 12, 2024
By Randy Osborne
News that Trevi Therapeutics Inc. got the size just right of the phase IIb Coral trial with Haduvio (oral nalbuphine extended release) led the company’s shares (NASDAQ:TRVI) to close Dec. 12 at $3.60, up $1.11, or 45%, after trading as high as $4.60.
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Line graph arrow trending upward

Wick-ed good phase III prostate cancer data light up Candel

Dec. 11, 2024
By Randy Osborne
Candel Therapeutics Inc. followed this spring’s positive phase II data in pancreatic cancer with favorable results from a phase III study testing the same drug – viral immunotherapy CAN-2409 – in localized prostate cancer. Shares of Needham, Mass.-based Candel (NASDAQ:CADL) closed Dec. 11 at $7.75, up $3.14, or 68%.
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Pediatric exam

Enanta logs phase II RSV win with zelicapavir

Dec. 9, 2024
By Randy Osborne
Enanta Pharmaceuticals Inc. hit the mark that Wall Street hoped for, and details rolled out in top-line results from the first-in-pediatrics phase II study evaluating once-daily, oral zelicapavir in hospitalized and non-hospitalized children aged 28 days to 36 months with respiratory syncytial virus (RSV).
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Illustration of tau accumulating in a neuron cell.

UCB/Roche lead Voyagers in Alzheimer’s tau campaign

Dec. 6, 2024
By Randy Osborne
Voyager Therapeutics Inc.’s recent selection of a lead development candidate, VY-1706, for its tau silencing gene therapy program in Alzheimer’s disease brought renewed attention to the target, which continues to intrigue a substantial lineup of developers. Bellwether data rolled out this fall from UCB SA and Roche AG at the Clinical Trials in Alzheimer’s Disease meeting in Madrid.
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Art concept for bladder

Protara, CG climb bladder ladder with SUO cancer findings

Dec. 5, 2024
By Randy Osborne
Among the drug developers with clinical results featured at the annual meeting of the Society for Urologic Oncology (SUO) in Dallas were Protara Therapeutics Inc. with phase II numbers and CG Oncology Inc. with a phase III update. Protara’s shares (NASDAQ:TARA) closed Dec. 5 at $6.02, up $2.48, or 70%, having traded as high as $10.48 during the day. Less reactive was stock in CG (NASDAQ:CGON), which ended at $33.56, down $2.35.
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Zepbound vials

Weight for it: Lilly wins, details later on Zepbound vs. Wegovy

Dec. 4, 2024
By Randy Osborne
Although head-to-head results on tolerability were missing from the company’s data release, Eli Lilly and Co. said its U.S. FDA-approved weight-loss drug Zepbound (tirzepatide) beat the also-cleared Novo Nordic A/S compound Wegovy (semaglutide) in a phase IIIb study comparing the two.
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Phase Ia interim data in prostate cancer boost Janux stock

Dec. 3, 2024
By Randy Osborne
Janux Therapeutics Inc. CEO David Campbell said the firm will be talking with the U.S. FDA about “what we may or may not be able to do [in order to get JANX-007] to patients more rapidly,” though he noted that the agency has “primarily been focused on overall survival” in considering prostate cancer drugs, so more work on that endpoint may be required. “We’ll keep that in mind,” he said.
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