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BioWorld - Tuesday, February 17, 2026
Home » Newsletters » BioWorld

BioWorld

July 19, 2019

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Bolstering IPF 'Bridge,' Boehringer signs potential €1.1 billion ATX inhibitor deal

Seongnam, Korea-based Bridge Biotherapeutics Inc. nailed down a deal with Boehringer Ingelheim GmbH (BI) to develop the former's phase I autotaxin (ATX) inhibitor, BBT-877, for fibrosing interstitial lung diseases, including idiopathic pulmonary fibrosis (IPF). Read More

Pharma investors return for Medicxi's $449M third fund

LONDON – Medicxi has closed a €400 million (US$449 million) third fund, bringing the amount raised by the venture capital firm since it split off from its parent Index Ventures three years ago, to more than $1 billion. Read More

Kronos makes time for series A financing, adds $105M with help from execs, board members

Kronos Bio Inc. closed a $105 million series A preferred stock financing, shored up by a board composed of longtime pharma executives that includes the company CEO and president, Norbert Bischofberger, the former Gilead Sciences Inc. R&D executive vice president and chief science officer. Read More

Singapore startup Aum bags triple-action cancer candidate in agreement with Inflection

HONG KONG – Singaporean biotech company Aum Biosciences Pte. Ltd. has in-licensed a potentially first-in-class PIM/PI3K/mTOR inhibitor from Inflection Biosciences Ltd., of Dublin and London, to develop it globally to treat a wide range of cancers. Read More

The fix isn't in yet, as prices, politics and pay-fors prolong passage of Rx remedy

The best way to score political points is to actually do something about U.S. prescription drug prices. That's the message members of the New Democrat Coalition Health Care Task Force delivered Wednesday to their party leadership in the House, as they requested another vote next week on a package of bipartisan drug pricing bills – this time minus the partisan provisions that Democrats knew would never fly in a Republican-controlled Senate. Read More

CD47 race heats up in China as I-Mab's antibody cleared for trials in advanced tumors

HONG KONG – China has approved the fourth homegrown CD47 antibody to start clinical trials, intensifying the local CD47 race. Chinese biologics developer I-Mab Biopharma (Shanghai) Co. Ltd. said it received the go-ahead for the clinical study of TJC-4, its differentiated fully human CD47 monoclonal antibody for treating advanced malignant tumors. Read More

Market uncertainty fails to slow biopharma IPO activity

Despite the ups and downs of the general markets and a U.S. government shutdown at the beginning of the year that contributed to no biopharma companies graduating to the public ranks in January, the enthusiasm for biopharma IPOs has remained steady since then. In fact, a flurry of IPO listings on U.S. stock exchanges last month helped bring the total of those offerings to 30 at the halfway point in the year.  Read More

Other news to note

Arvinas Inc., of New Haven, Conn., reported preclinical data on its tau-targeted Protac protein degrader program at the Alzheimer's Association International Conference in Los Angeles. After parenteral administration of the drug, more than 95% of pathologic tau protein was eliminated in the brain of a mouse tauopathy model. Read More

Financings

Obseva SA, of Geneva, said its board approved an increase of its share capital from 45.5 million shares to 48.6 million. The shares will be listed on the SIX Swiss Exchange on or around July 23. Read More

Clinical data for July 18, 2019

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Regulatory actions for July 18, 2019

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