Chipscreen Biosciences' Injectable NW001 Clinical Trial Application Accepted

Product / Tech
โดย 证券时报·CN·Read original
Summary · why it matters

Chipscreen Biosciences announced that the clinical trial application for injectable NW001, co-developed with Chengdu Chipscreen New Domain Biotechnology, for the treatment of advanced malignant tumors, including solid tumors and lymphoma, has received the Acceptance Notice for domestic production drug registration clinical trials issued by the Center for Drug Evaluation of the National Medical Products Administration.

Impact on stocks 1

Others · 1 stocks

Theme Impact 1

Off-coverage companies 1

成都微芯新域生物技术有限公司Private▲ Positive
Technologyrelevance

Co-developer of NW001, trial acceptance is a positive regulatory milestone.

Related news

Novo Rebrands as Novo, Lilly Wins FDA Nod, GE HealthCare Nears $1B Sofie Deal

Novo Nordisk will shorten its name to Novo and update its logo, with its trademark bull shifting to face right, as the Danish drugmaker battles Eli Lilly for dominance in the obesity-drug market. CEO Mike Doustdar is pushing to make Novo leaner and more competitive, and the company will detail its updated corporate strategy at a Capital Markets Day on September 21 in London. Separately, Eli Lilly said the U.S. FDA granted full approval for an all-oral regimen combining its estrogen receptor antagonist Inluriyo and kinase inhibitor Verzenio as a late-line option for adults with estrogen receptor-positive, HER2-negative breast cancer with an ESR1 mutation whose disease progressed after one or more prior endocrine therapies. GE HealthCare Technologies is in advanced talks to acquire Sofie Biosciences for about $1 billion, a deal that would expand its presence in radioactive diagnostic agents used with medical scans, according to the Financial Times. Summit Therapeutics said ivonescimab reduced the risk of death by 27% versus Merck's Keytruda in a late-stage lung cancer trial, with median overall survival of 30.8 months versus 22.6 months. Medtronic launched an exchange offer to split off at least 80.1% of MiniMed Group, allowing shareholders to exchange ordinary shares for MiniMed common stock at a 7% discount.
Seeking Alpha·1hRead more →

Eli Lilly Fair Value Rises to US$1,325.39 as Analysts Back GLP-1 Growth

Eli Lilly's updated fair value estimate has shifted from US$1,297.31 to US$1,325.39, with revenue growth moving from 13.98% to 14.17%, net profit margin from 41.26% to 42.01%, and future P/E from 28.66x to 28.85x, while the discount rate held at 7.24%. The revision sits alongside analyst price targets that often exceed US$900, with a cluster between US$1,300 and US$1,600, as firms including Citi, BMO Capital, RBC Capital, UBS, Morgan Stanley, Bernstein, Truist, Cantor Fitzgerald, BofA, Leerink and Berenberg raised targets into a range stretching from around US$1,135 to US$1,600. Guggenheim lifted its target to US$1,284, incorporating updated prescription and pricing assumptions and the reinstatement of Zepbound on the CVS formulary, while HSBC kept a Reduce rating even after raising its target to US$940, citing elevated sector multiples. The U.S. FDA granted full approval for Eli Lilly's Inluriyo in combination with Verzenio for adults with ER+, HER2-, ESR1-mutated advanced or metastatic breast cancer after progression on endocrine therapy, based on Phase 3 EMBER-3 data showing the combination doubled median progression-free survival versus Inluriyo alone. Eli Lilly also plans to present data on Mounjaro, Zepbound, Foundayo, retatrutide and eloraTZP at the European Association for the Study of Diabetes 2026 meeting in Milan, and Berenberg upgraded the stock citing weight-loss drug growth prospects, a pipeline described through 2030, and around US$60b committed to more than 25 business development deals this year, including acquisitions in sleep and cancer.
Simply Wall St·10hRead more →

Agenus Fair Value Rises to US$26.33 on Trial Updates and Fresh Financing

Agenus now carries an updated implied fair value of about US$26.33 per share, up from US$19.50, a roughly 35% increase tied to trial updates and fresh financing. The higher target reflects recent Street commentary on the botensilimab plus balstilimab program in microsatellite stable colorectal cancer and on new capital that changes how investors weigh financing risk. Chardan, H.C. Wainwright and B. Riley have all assigned Buy ratings on the stock in 2026, with price target revisions to US$30, US$25 and US$14. H.C. Wainwright factors in an assumed issuance of 23 million shares tied to an US$85 million upfront financing payment, highlighting ongoing dilution and funding risk. The fair value update also reflects revenue growth assumptions of a decline of about 1.37%, a net profit margin easing from about 17.91% to about 17.63%, a future P/E shifting from about 58.6x to about 80.6x, and a discount rate moving from about 7.60% to about 7.69%.
Simply Wall St·12hRead more →