novartis Boston Biotech Announces Novartis Collaboration By www.streetwisereports.com Published On :: Mon, 28 Oct 2024 00:00:00 PST Source: Dr. Robert Driscoll 10/28/2024 Monte Rosa Therapeutics Inc. (GLUE:NASDAQ) recently unveiled a collaborative agreement with Novartis for the development of MRT-6160, its VAV1-degrader program, according to a Wedbush research note.Wedbush analysts Dr. Robert Driscoll, Dr. Ritika Das, and Sam Ravina, in a research report published on October 28, 2024, maintained their Outperform rating on Monte Rosa Therapeutics Inc. (GLUE:NASDAQ) while raising their price target to US$15.00 from US$11.00. The report follows Monte Rosa's announcement of a collaborative agreement with Novartis for the development of MRT-6160, its VAV1-degrader program. The analysts highlighted the significant financial terms of the agreement, stating, "GLUE will receive an upfront payment of US$150M as well as total milestone payments of up to US$2.1B that will include US$1.5B in potential development and regulatory milestones that begin upon Ph 2 studies." Regarding the partnership structure, the analysts noted, "Upon start of Ph 3 studies, 30% US P&L would be shared with Ph 3 development co-fund and ex-US tiered royalties. Importantly, NVS will cover the complete costs of Ph 2 studies and will obtain worldwide rights to develop, commercialize and manufacture MRT-6160 as well as other VAV MGDs." The analysts viewed this collaboration positively, stating, "We view this favorable collaboration agreement as an additional robust validation of GLUE's QuEEN MGD platform (noting Novartis' significant efforts in the degrader space), as well as an acknowledgment of the significant potential opportunities around targeting VAV1 with a first in class degrader." They also emphasized the strategic benefits, noting, "Furthermore, we note the likely accelerated timelines for the MRT-6160 development program overall, and significant extension of GLUE's operational cash runway, which we expect to allow advancement of its deep pipeline." The report highlighted the ongoing Phase 1 SAD/MAD healthy subject study for MRT-6160 in autoimmune diseases, with initial data expected in 1Q:25. Wedbush's valuation methodology is based on sales multiples. The analysts explained, "Our PT is derived from applying a 6x multiple to estimated US sales and a 15x multiple to EU royalties of MRT-2359 in 2031, discounted by 30% annually." The analysts also outlined several risk factors, including potential clinical and regulatory failure of MRT-2359, challenges in achieving sales estimates, and possible commercial competition from current and future therapies. In conclusion, Wedbush's increased price target to US$15 reflects growing confidence in Monte Rosa Therapeutics following the Novartis collaboration agreement. The share price at the time of the report of US$8.05 represents a potential return of approximately 86% to the analysts' target price, highlighting the significant upside potential as the company advances its development programs with its new partner. 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For additional disclosures, please click here. Disclosures for Wedbush, Monte Rosa Therapeutics Inc., October 28, 2024 Analyst Certification We, Robert Driscoll, Ritika Das and Sam Ravina, certify that the views expressed in this report accurately reflect our personal opinions and that we have not and will not, directly or indirectly, receive compensation or other payments in connection with our specific recommendations or views contained in this report. The Distribution of Ratings is required by FINRA rules; however, WS' stock ratings of Outperform, Neutral, and Underperform most closely conform to Buy, Hold, and Sell, respectively. Please note, however, the definitions are not the same as WS' stock ratings are on a relative basis. The analysts responsible for preparing research reports do not receive compensation based on specific investment banking activity. The analysts receive compensation that is based upon various factors including WS' total revenues, a portion of which are generated by WS' investment banking activities. Company Specific Disclosures This information is subject to change at any time. 2. WS managed a public offering of securities for Monte Rosa Therapeutics within the last 12 months. 4. WS has received compensation for investment banking services from Monte Rosa Therapeutics within the last 12 months. 5. WS provided Monte Rosa Therapeutics with investment banking services within the last 12 months. Wedbush disclosure price charts are updated within the first fifteen days of each new calendar quarter per FINRA regulations. Price charts for companies initiated upon in the current quarter, and rating and target price changes occurring in the current quarter, will not be displayed until the following quarter. Additional information on recommended securities is available on request. 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( Companies Mentioned: GLUE:NASDAQ, ) Full Article
novartis AG Jennings announces settlement with Novartis regarding allegations of improper kickbacks By news.delaware.gov Published On :: Mon, 21 Sep 2020 17:10:28 +0000 Attorney General Kathy Jennings announced Monday that Delaware has joined the United States, twenty-seven other states, and the District of Columbia to settle allegations against Novartis Pharmaceuticals Corporation (“Novartis”). Delaware’s settlement amount of $94,450.99 will go to the Division of Medicaid and Medicaid Assistance (“DMMA”) within the Delaware Department of Health and Social Services (“DHSS”). […] Full Article Department of Justice Department of Justice Press Releases News
novartis Mariana Oncology’s Radiopharm Platform Acquired By Novartis By lifescivc.com Published On :: Mon, 06 May 2024 10:42:46 +0000 Novartis recently announced the acquisition of Mariana Oncology, an emerging biotech focused on advancing a radioligand therapeutics platform, for up to $1.75 billion in upfronts and future milestones. The capstone of its three short years of operations, this acquisition represents The post Mariana Oncology’s Radiopharm Platform Acquired By Novartis appeared first on LifeSciVC. Full Article Exits IPOs M&As Leadership Portfolio news Talent #RLT Mariana Oncology Novartis radioligand therapy Radiopharm
novartis Novartis announces FDA approval for Jadenu� to simplify treatment administration for patients with chronic iron overload - Dr. Elliott Vichinsky on Jadenu By www.multivu.com Published On :: 31 Mar 2015 13:15:00 EDT Elliott Vichinsky, MD, University of California, San Francisco (UCSF) Benioff Children's Hospital Oakland Full Article Healthcare Hospitals Medical Pharmaceuticals Pharmaceuticals New Products Services Broadcast Feed Announcements FDA Approval MultiVu Video
novartis Elanco Finalizes Acquisition of Novartis Animal Health India By www.medindia.net Published On :: Animal health products and knowledge services firm Elanco has more than 100 product development projects focused on life extension of pets, pet care, Full Article
novartis Novartis Launches Scapho Drug for the Treatment of Psoriasis By www.medindia.net Published On :: Switzerland-based pharmaceutical company, Novartis has launched the drug, Scapho for the treatment of plaque psoriasis in India. Psoriasis is a severe, Full Article
novartis Dr. Reddy’s closes acquisition of Novartis’ Habitrol brand By www.thehindu.com Published On :: Fri, 19 Dec 2014 12:21:38 +0530 Full Article Industry
novartis Novartis, Dr. Reddy’s in exclusive sales pact for select products By www.thehindu.com Published On :: Fri, 11 Feb 2022 11:38:00 +0530 400 Novartis employees to lose jobs due to resulting role redundancies Full Article Business
novartis Novartis to end anti-infectives R&D By cen.acs.org Published On :: 13 Jul 2018 15:34:00 +0000 Full Article
novartis T.H. v. Novartis Pharmaceuticals Corporation By feeds.findlaw.com Published On :: 2017-12-21T08:00:00+00:00 (Supreme Court of California) - Affirming the Court of Appeals determination that the manufacturer of a name brand drug whose labeling directs the warnings provided on its generic bioequivalent's packaging owes a duty of reasonable care to the consumers of the generic drug and that the liability for potential negligence doesn't automatically terminate upon transfer of the company's rights in the name brand drug to a successor manufacturer. Full Article Injury & Tort Law Drugs & Biotech Product Liability
novartis United Food and Commercial Workers Unions v. Novartis Pharmaceutical Corp. By feeds.findlaw.com Published On :: 2018-08-21T08:00:00+00:00 (United States First Circuit) - Affirmed the dismissal of two putative antitrust class actions alleging that a pharmaceutical company took steps to block the entry of generic versions of its leukemia-treatment drug into the U.S. market. The plaintiffs, including several labor union benefit funds, claimed that the drugmaker engaged in anticompetitive conduct by bringing sham infringement lawsuits against manufacturers trying to enter the market with generic versions of that drug. Dismissing the complaints, the district court held that the plaintiffs had not plausibly alleged their claims, and the First Circuit affirmed. Full Article Antitrust & Trade Regulation Health Law Drugs & Biotech
novartis United Food and Commercial Workers Unions v. Novartis Pharmaceutical Corp. By feeds.findlaw.com Published On :: 2018-08-21T08:00:00+00:00 (United States First Circuit) - Affirmed the dismissal of two putative antitrust class actions alleging that a pharmaceutical company took steps to block the entry of generic versions of its leukemia-treatment drug into the U.S. market. The plaintiffs, including several labor union benefit funds, claimed that the drugmaker engaged in anticompetitive conduct by bringing sham infringement lawsuits against manufacturers trying to enter the market with generic versions of that drug. Dismissing the complaints, the district court held that the plaintiffs had not plausibly alleged their claims, and the First Circuit affirmed. Full Article Antitrust & Trade Regulation Health Law Drugs & Biotech
novartis United Food and Commercial Workers Unions v. Novartis Pharmaceutical Corp. By feeds.findlaw.com Published On :: 2018-08-21T08:00:00+00:00 (United States First Circuit) - Affirmed the dismissal of two putative antitrust class actions alleging that a pharmaceutical company took steps to block the entry of generic versions of its leukemia-treatment drug into the U.S. market. The plaintiffs, including several labor union benefit funds, claimed that the drugmaker engaged in anticompetitive conduct by bringing sham infringement lawsuits against manufacturers trying to enter the market with generic versions of that drug. Dismissing the complaints, the district court held that the plaintiffs had not plausibly alleged their claims, and the First Circuit affirmed. Full Article Antitrust & Trade Regulation Health Law Drugs & Biotech
novartis China approves Novartis' multiple sclerosis treatment Mayzent By news.yahoo.com Published On :: Sat, 09 May 2020 03:29:42 -0400 BEIJING (Reuters) - Chinese regulators have approved Novartis' Mayzent to treat relapsing multiple sclerosis in adults, the Swiss drug maker said in a statement on Saturday. Other drugs approved by China's National Medical Products Administration to treat MS include Novartis' Gilenya, Bayer's Betaferon and Sanofi's Aubagio. China has an estimated 30,000 patients with MS. (Reporting by Roxanne Liu and Kevin Yao in Beijing; Editing by Edwina Gibbs Full Article
novartis Speedy US approval for Novartis' Tabrecta By www.pharmatimes.com Published On :: Wed, 06 May 2020 22:47:33 +0100 The approval gives NSCLC patients whose tumours carry the MET exon 14 skipping mutation a new treatment option Full Article
novartis Novartis Drug Wins FDA Approval for Lung Cancers With Specific Mutation By xconomy.com Published On :: Thu, 07 May 2020 01:46:05 +0000 As cancer research reveals the genetic basis of the disease, pharmaceutical companies are pursuing targeted therapies that address certain groups of patients. One such drug from Novartis won FDA approval Wednesday, making it the first therapy cleared by the agency to treat patients whose non-small cell lung cancer (NSCLC) carries a certain genetic mutation. The […] Full Article National National blog main American Cancer Society Biotech cancer Cancer Drugs clinical trials companion diagnostic FDA Foundation Medicine Incyte kinase inhibitor Life Sciences myelofibrosis Novartis ruxolitinib
novartis Why Former Novartis CEO Joe Jimenez Joined A Microbiome Startup’s Board By www.forbes.com Published On :: Fri, 21 Sep 2018 11:00:00 +0000 uBiome, a San Francisco startup that sells commercial tests that use DNA sequencing to identify what microbes are in a person's stool or, for one test, in the vagina, has raised $83 million from venture capitalists to fund an entrée into drug development. Full Article ticker=NYSE:NVS byline=Matthew Herper
novartis Novartis acquires digital therapeutics specialist Amblyotech By www.outsourcing-pharma.com Published On :: Tue, 28 Apr 2020 15:39:00 +0100 The pharmaceutical firm has purchased the company, which specializes in advancing treatments and diagnostics for ocular disorders. Full Article Markets & Regulations
novartis EU approval for Novartis' Cosentyx in active non-radiographic axial spondyloarthritis By www.pharmafile.com Published On :: Wed, 29 Apr 2020 09:28:04 +0000 Novartis has revealed that the European Commission has moved to approve Cosentyx (secukinumab) for the treatment of active non-radiographic axial spondyloarthritis (nr-axSpA) in adult patients. Full Article axial spondyloarthritis Cosentyx EU Novartis pharma Research and Development Sales and Marketing
novartis Novartis’ asthma triple heads CHMP’s latest meeting By www.pmlive.com Published On :: Tue, 05 May 2020 12:50:48 +0100 Eight new medicines recommended for approval Full Article
novartis Novartis announces plan to initiate clinical trial of canakinumab for patients with COVID-19 pneumonia By www.pharmanews.eu Published On :: Wed, 29 Apr 2020 10:00:00 +0200 Novartis announced plans to initiate a Phase III clinical trial to study canakinumab in patients with COVID-19 pneumonia. The CAN-COVID trial will examine the efficacy of utilizing canakinumab, an interleukin (IL)-1β blocker, to treat a type of severe immune overreaction called cytokine release syndrome (CRS) in people with COVID-19 pneumonia. Full Article Featured Novartis Business
novartis Novartis taps real-life Cosentyx patients to thank healthcare workers, pledge patient support By www.fiercepharma.com Published On :: Sat, 02 May 2020 21:13:54 +0000 Novartis is using familiar faces—real patients from its Cosentyx TV commercials—to thank healthcare workers and promise support for patients. It’s a shift away from product-centered TV ads as Novartis adjusts its Cosentyx DTC effort during the COVID-19 crisis to highlight resources for patients, the drugmaker said. Full Article
novartis China approves Novartis' multiple sclerosis treatment Mayzent By feeds.reuters.com Published On :: Sat, 09 May 2020 03:29:42 -0400 Chinese regulators have approved Novartis' Mayzent to treat relapsing multiple sclerosis in adults, the Swiss drug maker said in a statement on Saturday. Full Article healthNews
novartis Novartis Vaccines & Diagnostics to Pay More Than $72 Million to Resolve False Claims Act Allegations Concerning TOBI By www.justice.gov Published On :: Tue, 4 May 2010 16:28:00 EDT Novartis Vaccines & Diagnostics Inc. and Novartis Pharmaceuticals Corporation have agreed to pay $72.5 million to resolve civil False Claims Act allegations arising from the marketing of the cystic fibrosis drug TOBI. Full Article OPA Press Releases
novartis Novartis Pharmaceuticals Corp. to Pay More Than $420 Million to Resolve Off-label Promotion and Kickback Allegations By www.justice.gov Published On :: Thu, 30 Sep 2010 14:28:32 EDT Novartis Pharmaceuticals Corporation has agreed to pay $422.5 million to resolve criminal and civil liability arising from the illegal marketing of certain pharmaceutical products. Full Article OPA Press Releases
novartis United States Files Complaint Against Novartis Pharmaceuticals Corp. for Allegedly Paying Kickbacks to Doctors in Exchange for Prescribing Its Drugs By www.justice.gov Published On :: Fri, 26 Apr 2013 15:19:31 EDT The Justice Department announced today that the United States has filed a second civil false claims lawsuit against Novartis Pharmaceuticals Corp. involving alleged kickbacks paid by the company to health care providers. Full Article OPA Press Releases
novartis Novartis announces FDA approval for Jadenu™ to simplify treatment administration for patients with chronic iron overload - Dr. Elliott Vichinsky on Jadenu By feedproxy.google.com Published On :: 31 Mar 2015 13:15:00 EDT Elliott Vichinsky, MD, University of California, San Francisco (UCSF) Benioff Children's Hospital Oakland Full Article Healthcare Hospitals Medical Pharmaceuticals Pharmaceuticals New Products Services Broadcast Feed Announcements FDA Approval MultiVu Video
novartis China approves Novartis' multiple sclerosis treatment Mayzent By feeds.reuters.com Published On :: Sat, 09 May 2020 12:59:42 +0530 Chinese regulators have approved Novartis' Mayzent to treat relapsing multiple sclerosis in adults, the Swiss drug maker said in a statement on Saturday. Full Article health
novartis Dried blood spots : applications and techniques / edited by Wenkui Li, Novartis Institutes for BioMedical Research, East Hanover, NJ, USA, Mike S. Lee, Milestone Development Service, Newtown, PA, USA By prospero.murdoch.edu.au Published On :: Full Article
novartis Orionis Biosciences launches with Novartis pact By feedproxy.google.com Published On :: 07 Mar 2020 11:22:39 +0000 Full Article
novartis Novartis to end anti-infectives R&D By feedproxy.google.com Published On :: 13 Jul 2018 15:34:00 +0000 Full Article