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BioWorld - Sunday, March 29, 2026
Breaking News: Trump administration impacts continue to roil the life sciences sectorBreaking News: Trump administration impacts continue to roil the life sciences sector
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BioWorld, Clinical
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Coronavirus and DNA

Coronavirus waylays China trials, may delay regulatory approvals too

Feb. 18, 2020
By Elise Mak
BEIJING – Multiple China-based clinical trials have been put on hold as the country concentrates on its fight against COVID-19. To curb the spread of the novel coronavirus that has infected over 72,000 people and killed nearly 2,000, China has imposed travel and transport restrictions, making trips difficult or even impossible for patients and physicians.
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Lungs wireframe illustration

Bellerophon shares blast off with new Inopulse data

Feb. 18, 2020
By Michael Fitzhugh
Shares of Bellerophon Therapeutics Inc. (NASDAQ:BLPH), rescued from potential delisting by a recent reverse stock split, shot 168.4% higher to $9.20 on Feb. 18 as new top-line data from a small phase II study showed its inhaled nitric oxide delivery system, Inopulse, delivered significant improvements in blood flow for people with pulmonary hypertension (PH) associated with pulmonary fibrosis (PF).
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Doctor examining patient's hand
Newco news

Zhittya gains approval for phase I Parkinson’s trial in Mexico

Feb. 14, 2020
By Lee Landenberger
Privately held Zhittya Genesis Medicine Inc. received approval from Mexico’s Comisión Federal para la Protección contra Riesgos Sanitarios (Cofepris) to begin a phase I trial at the Zambrano Hospital in Monterrey for patients with Parkinson’s disease.
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Syringe and ampoules

Sanifit seeks benefit in pivotal trial for rare calcification disorder

Feb. 14, 2020
By Michael Fitzhugh
Spain's Sanifit Laboratoris SL, a company developing treatments for calcification disorders, has dosed the first patient in a phase III trial of its lead asset, SNF-472, for the treatment of the rare and sometimes deadly disease calciphylaxis, a calcium accumulation disorder.
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Hoth touts preliminary data on lupus skin disease candidate

Feb. 12, 2020
By Michael Fitzhugh
New York-based Hoth Therapeutics Inc. said preliminary preclinical data on a topical nanoparticle formulation of the endocannabinoid anandamide it licensed from Zylö Therapeutics Inc. represents "a positive step toward underlining the transformative potential" of the early stage therapy for the skin disease cutaneous lupus erythematous.
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Logicbio shares sink as FDA hold delays plans to launch phase I/II trial

Feb. 11, 2020
By Michael Fitzhugh
Pediatric gene editing specialist Logicbio Therapeutics Inc. has revealed an FDA clinical hold on a planned phase I/II trial of its lead candidate, LB-001, an investigational therapy for rare inherited metabolic disorder methylmalonic acidemia (MMA).
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Roche, Lilly drugs fail to slow decline in early onset AD

Feb. 10, 2020
By Michael Fitzhugh
A high-profile test of two experimental medicines in people with autosomal dominant Alzheimer’s disease (ADAD), a rare inherited form of the disease, found that neither drug significantly slowed rates of cognitive decline vs. placebo, the primary endpoint.
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Anxious balance: Biohaven’s troriluzole misses its primary endpoint while rimegepant could be a blockbuster

Feb. 10, 2020
By Lee Landenberger
Top-line results from Biohaven Pharmaceutical Holding Co.’s phase III trial of troriluzole against placebo in treating generalized anxiety disorder (GAD) failed to hit its primary endpoint, prompting the company CEO to say the poor results support halting development plans for the glutamate modulator as a monotherapy in GAD.
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Diabetes glucose monitor

Vtv scores phase II TD in T1D as Alzheimer’s bid RAGEs against dying of light

Feb. 10, 2020
By Randy Osborne
With the Simpliciti-T1 phase II trial testing new-mechanism TTP-399 as adjunct therapy in type 1 diabetes (T1D), High Point, N.C.-based Vtv Therapeutics Inc. nailed the HbA1c endpoint with none of the safety concerns foiling developers of type 2 diabetes (T2D) drugs who sought to broaden their labels.
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Oculis’ topical DME drug hits phase II endpoints, validates nanoparticle delivery solution

Feb. 10, 2020
By Nuala Moran
LONDON – Oculis SA reported positive results for its topical nanoparticle formulation of dexamethasone in the treatment of diabetic macular edema (DME), showing the eye drops reduced central macular thickness (CMT) in the phase II proof-of-concept trial.
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