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BioWorld - Wednesday, April 15, 2026
Home » Authors » Randy Osborne

Randy Osborne

Articles

ARTICLES

To B or not to B: Corvus’ new approach takes arms against COVID-19

July 7, 2020
By Randy Osborne
Corvus Pharmaceuticals Inc.’s success in treating a COVID-19 patient previously diagnosed with non-small-cell lung cancer (NSCLC) with CPI-006 helped boost shares (NASDAQ:CRVS) to $4.96, up $2.21, or 181%, as the Burlingame, Calif.-based company disclosed the start of a phase I study to investigate the anti-CD73 immunotherapy prospect.
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No holiday in UF walk down Primrose lane; Obseva shares melty on Yselty

July 6, 2020
By Randy Osborne
Geneva-based Obseva SA’s top-line data from the pivotal phase III studies called Primrose 1 and 2 with GnRH antagonist Yselty (linzagolix) pleased the company, but Wall Street not so much.
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Coin stacks, dollar signs and up arrow

Agonist ecstasy? HER2 (and more) ‘Bolt’-on strategy draws $93.5M series C

July 1, 2020
By Randy Osborne
Bolt Biotherapeutics Inc.’s $93.5 million series C round “takes us well into the back end of 2021 and into 2022,” CEO Randall Schatzman told BioWorld, with enough money that the firm is “not impeded in terms of the creativity [we’re] bringing to the table.”
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FDA Not Approved stamp

Heron knocked by second CRL for postoperative pain drug

June 29, 2020
By Randy Osborne
Shares of Heron Therapeutics Inc. sank 27% in morning trading, after the San Diego-based firm disclosed a second complete response letter (CRL) for HTX-011 in postoperative pain. The CRL, received from the FDA on June 26, the anticipated PDUFA date, stated the agency was unable to approve the NDA in its present form and called for additional nonclinical information.
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IPO, coins, financial chart

Twin peaks: Akouos, Fusion go high in matching $212M IPOs

June 26, 2020
By Randy Osborne
A pair of upsized IPOs packed away cash by way of identical terms, with Boston-based Akouos Inc. and Fusion Pharmaceuticals Inc., of Hamilton, Ontario, separately selling 12.5 million shares at $17 each for $212.5 million in gross proceeds.
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Opaganib bottle and tablets

Yeliva see anything: Redhill calls out opaganib’s promise in COVID-19

June 24, 2020
By Randy Osborne
Redhill Biopharma Ltd.’s chief operating officer, Gilead Raday, told BioWorld that the firm will build on positive results in severe COVID-19 patients with oral opaganib, a first-in-class sphingosine kinase-2 inhibitor.
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Vikram Sudarsan, CEO, Engrail Therapeutics

Everybody Nan Fung: China backer high profile as Engrail unveiled with $32M series A

June 23, 2020
By Randy Osborne
Nan Fung Life Sciences is “looking to make a significant presence in the field,” said Engrail Therapeutics Inc. CEO Vikram Sudarsan, whose firm bagged a $32 million series A round led by the global investment platform of Hong Kong’s Nan Fung Group, and its support represents “a clear statement in that direction.”
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Zynerba says FDA ‘alert, listening’ to broadened spectrum of autism therapy

June 22, 2020
By Randy Osborne
Zynerba Pharmaceuticals Inc. in late May popped the lid off top-line data from the open-label phase II study called Bright with ZYN-002 in children and adolescents with autism spectrum disorder, and the findings drew adjectives from Wall Street such as “provocative” and “encouraging.”
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Vikram Sudarsan, CEO, Engrail Therapeutics

Everybody Nan Fung: China backer high profile as Engrail unveiled with $32M series A

June 18, 2020
By Randy Osborne
Nan Fung Life Sciences is “looking to make a significant presence in the field,” said Engrail Therapeutics Inc. CEO Vikram Sudarsan, whose firm bagged a $32 million series A round led by the global investment platform of Hong Kong’s Nan Fung Group, and its support represents “a clear statement in that direction.”
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Tazverik product image

Back for seconds, Epizyme served up FDA go-ahead for Tazverik in FL

June 18, 2020
By Randy Osborne
About six months after Epizyme Inc. won FDA clearance of Tazverik (tazemetostat) for epithelial sarcoma (ES), the firm scored accelerated approval in the larger indication of relapsed or refractory (r/r) follicular lymphoma (FL). Specifically, U.S. regulators cleared the methyltransferase inhibitor for adults whose tumors test positive for an EZH2 mutation who have received at least two prior systemic therapies and for those with no satisfactory alternative treatment options – language that “gives physicians a lot of flexibility to use their clinical judgement in how to best prescribe” the drug, CEO Robert Bazemore noted.
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