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BioTuesdays

9 Meters Biopharma targeting rare and unmet needs in GI disorders

9 Meters Biopharma (NASDAQ: NMTR) expects to report clinical trial data readouts in 2021 from two gastrointestinal disorders: short bowel syndrome, an underserved and debilitating rare disease, and celiac disease, an autoimmune disorder with a genetic link.

Silencing gene expression to cure complex diseases

Immuneering uses bioinformatics to develop new medicines while also helping large pharmaceutical companies improve their treatments.

Woburn-based biotech company seeing promising results in COVID-19 antibody treatment

A Woburn-based biotech company says it’s seeing early success with COVID-19 antibody treatments. Scientists at Abpro have been studying antibodies for a decade but the CEO says this research hits differently.

Execs Weigh In On Presidential Politics Impacting Biopharma

We at NeuBase have felt that there are fundamental deficiencies in the current approach to drug development. The traditional drug screening approach, which involves scouring libraries of chemicals and just seeing what works, is slow, costly, and ultimately translates to higher drug prices. We believe that there will be a revolution in the pharmaceutical industry that leverages the power of the digital age.

Fox Business

Immunitybio to begin phase one testing of COVID-19 vaccine candidate

Immunitybio Chairman and CEO Dr. Patrick Soon-Shiong joins ‘Maria Bartiromo’s Wall Street’ to discuss

endpoints

Promising better linker tech to ADC field, Araris has ‘very, very ambitious’ plans for the clinic

A couple months after raising CHF 2.5 million ($2.76 million) in initial seed funding, one-year-old Araris Biotech is topping off the round with another CHF 12.7 million ($14 million).

Ensuring Patient-Friendly Clinical Trials For Complex Disorders — A Small Biopharma’s Playbook

Rezolute, a small company based in Redwood City, California, and working in the rare pediatric disease space, is developing a new therapeutic option specifically for patients with congenital hyperinsulinism (HI), an ultra-rare pediatric genetic disorder. For Rezolute, connecting and partnering with advocacy groups and physicians is paramount in clinical trial execution.

First Person Treated in Amolyt Pharma’s AZP-3601 Trial for Hypoparathyroidism

Amolyt Pharma, formerly Alizé Pharma 3, had announced earlier this year its plans to start a clinical trial of AZP-3601 by the end of 2020.