Sarah de Crescenzo, Xconomy

Sarah de Crescenzo

Xconomy

San Diego, CA, United States

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Recent:
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Past:
  • Xconomy

Past articles by Sarah:

Xconomy: AbbVie & UroGen Overactive Bladder Treatment Misses in Phase 2 Trial

A formulation of AbbVie’s blockbuster wrinkle treatment, acquired through its buyout of Allergan, has failed a mid-stage trial as a potential fix for → Read More

Xconomy: Kinnate Raises $98M for Human Tests of Targeted Cancer Therapies

Drugs designed to precisely target cancers with specific genetic signatures have changed the course of disease for many patients. But for the majority, → Read More

Xconomy: Freenome Tacks on $270M to Advance Blood Tests to Find Cancer Early

The ability to detect early signs of cancer in a patient’s blood could improve prognoses by helping doctors treat the disease before symptoms arise. → Read More

Xconomy: Acadia Pharma Acquires CerSci, Potential Pain Meds in $52.5M Buyout

Acadia Pharmaceuticals has acquired Texas biotech CerSci Therapeutics, a privately held company with a clinical-stage molecule under evaluation as a → Read More

Xconomy: FDA Adds Plasma as 2nd COVID-19 Treatment Under Emergency Guidelines

The FDA has authorized the use of plasma from people who have recovered from infection by the novel coronavirus as a treatment for hospitalized COVID-19 → Read More

Xconomy: Bio Roundup: J&J Buyout, BioMarin Rebuffed, Poseida on Hold & More

While business is historically slow in August, this month seems to be bucking the trend, just like so many other unexpected developments in 2020. Perhaps → Read More

Xconomy: Harmony Bio and Inhibrx Raise Combined $247M in Public Market Debuts

Two biotechs this week topped the $100 million mark in their respective initial public offerings, both of which were able to offer more shares than → Read More

Xconomy: FDA Rejects BioMarin Hemophilia Gene Therapy, Asks for More Data

A gene therapy designed to treat the severest cases of the most common type of hemophilia has been rejected by the FDA, which wants more data on the → Read More

Xconomy: Patient Death in Poseida Prostate Cancer Study Prompts Clinical Hold

A Phase 1 trial testing a Poseida Therapeutics cell therapy in men with prostate cancer is on hold after a patient enrolled in the study died of liver → Read More

Xconomy: Genentech Gets FDA OK for Injectable Rare Neuroimmune Disease Drug

A drug that can be administered at home to treat a rare central nervous system disorder that damages the optic nerves and spinal cord now has FDA → Read More

Xconomy: Tango Therapeutics Adds $175M, Deal Turns Partner Gilead Into Investor

Cancer drug developer Tango Therapeutics is adding $175 million more to its coffers in cash and equity, funds the company says will help it get its lead → Read More

Xconomy: Bristol Myers Squibb to Splash Out $475M on Dragonfly Immunotherapy

Bristol Myers Squibb is paying nearly half a billion dollars in up front and near-term payments to license an early-stage immunotherapy developed by → Read More

Xconomy: Advisory Body Backs MesoBlast Therapy for Transplant Complication

An FDA advisory committee Thursday voted 9-1 to recommend that the agency approve a stem cell therapy developed by MesoBlast as a treatment for acute → Read More

Xconomy: Perceptive Advisors’ LianBio Inks Deals With BridgeBio, MyoKardia

Two California biotechs have teamed up with LianBio, a new company launched earlier this week by hedge fund Perceptive Advisors, as part of deals that → Read More

Xconomy: Ligand to Spend $438M to Add Protein Maker Pfenex to Technology Lineup

Ligand Pharmaceuticals plans to acquire recombinant protein therapeutics maker Pfenex for $438 million, the companies announced Monday. The larger company → Read More

Xconomy: Roche Gut Disease Drug Produces Mixed Results in Late-Stage Trials

Results from four studies within a major Roche-run clinical trials program of an investigational gut disease drug have muddled the antibody’s path forward → Read More

Xconomy: FDA Green-Lights Roche Spinal Muscular Atrophy Drug, First Oral Therapy

The FDA on Friday approved a new spinal muscular atrophy drug that patients can take at home. Risdiplam (Evrysdi) is a liquid medicine intended for daily → Read More

Xconomy: Bio Roundup: A Telehealth Combo, FDA's BCMA OK, Biogen's Bet & More

The novel coronavirus has driven the pharmaceutical industry to upend its research priorities. Big Pharma companies are focusing on vaccine development → Read More

Xconomy: GlaxoSmithKline Multiple Myeloma Drug Earns FDA’s First Anti-BCMA Nod

Patients with advanced multiple myeloma have a new treatment option with the FDA’s approval of a GlaxoSmithKline drug that targets B-cell maturation → Read More

Xconomy: G1 Vets Launch Arc Therapeutics to Take on New Cancer Target

Three early employees of G1 Therapeutics have launched a new oncology-focused company and raised $6 million to move a preclinical program licensed from → Read More