Novartis

Novartis AG is a holding company, which engages in the development, manufacture, and marketing of healthcare products. It operates through the following segments: Innovative Medicines, Sandoz, and Corporate. The Innovative Medicines segment researches, develops, manufactures, distributes and sells patented pharmaceuticals, and is composed of two business units: Novartis Oncology and Novartis Pharmaceuticals. The Sandoz segment develops, manufactures and markets finished dosage form medicines as well as intermediary products, including active pharmaceutical ingredients. The Corporate segment refers to group management and central services. The company was founded on February 29, 1996 and is headquartered in Basel, Switzerland.

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Novartis AG is a holding company, which engages in the business of developing, manufacturing, and marketing healthcare products. It operates through the following segments: Innovative Medicines, Sandoz, and Corporate. The Innovative Medicines segment includes researching, distributing and selling patented pharmaceuticals. The Sandoz segment focuses on marketing finished dosage form medicines and intermediary products including active pharmaceutical ingredients. The Corporate segment is involved in group management and central services. The company was founded on February 29, 1996 and is headquartered in Basel, Switzerland.

Basel, April 5, 2022 – Novartis today announced the U.S. Food and Drug Administration (FDA) has granted commercial licensure approval for its Durham, N.C. site, a multi-product gene therapy manufacturing facility. This approval allows the state-of-the-art, 170,000 square-foot facility to make, test and release commercial Zolgensma, as well as produce gene therapy product for current and future clinical trials.

Novartis expands Zolgensma manufacturing capacity with approval of multi-product North Carolina facility

Novartis said on Monday it was integrating its pharmaceuticals and oncology units into an innovative medicines (IM) business to simplify its structure, targeting savings of at least $1 billion by 2024.

Novartis integrates pharmaceuticals and oncology, targets savings of $1 billion

Ad hoc announcement pursuant to Art. 53 LR

Novartis announces new organizational structure to accelerate growth, strengthen pipeline and increase productivity

Novartis (NVS) ophthalmology drug Beovus label gets expanded in EU for diabetic macular edema.

Novartis (NVS) Beovu Gets Label Expansion for DME in EU

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Novartis (NVS) obtains positive CHMP opinion for the label expansion of Jakafi and Kymriah.

Novartis (NVS) Gets Positive CHMP Opinion for Jakafi, Kymriah

Basel, March 25, 2022 — Novartis announced today that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion recommending the European Commission to approve Kymriah® (tisagenlecleucel), a CAR-T cell therapy, for the treatment of adult patients with relapsed or refractory (r/r) follicular lymphoma (FL) after two or more lines of systemic therapy.

Novartis receives positive CHMP opinion for Kymriah® CAR-T cell therapy for adult patients with relapsed or refractory follicular lymphoma in Europe

The FDA okays Novartis' (NVS) targeted radioligand therapy Pluvicto to treat PSMA-positive metastatic castration-resistant prostate cancer.

Novartis' (NVS) Pluvicto Gets FDA Nod for Advanced Prostate Cancer

Swiss drugmaker Novartis said on Tuesday it was suspending capital investments, media advertising, and other promotional activities in Russia but remained committed to providing access to its medicine there.

Novartis suspends some business activities in Russia

Stability is one of the things we'll want to look for in this unstable environment. I've invested tens of thousands into Novartis.

Novartis: Exceedingly Stable Swiss Pharma

Novartis (NVS) reports positive data on SMA treatment from a phase III study. It also acquires Coalesce Product Development Limited to strengthen its respiratory and complex generics business.

Novartis (NVS) Announces Data on Zolgensma, Acquires Coalesce

Novartis AG (NYSE: NVS) announced new data from the completed Phase 3 SPR1NT study of Zolgensma (onasemnogene abeparvovec), a one-time treatment for spinal muscular atrophy (SMA).  The data demonstrated that children with three copies of the SMN2 backup gene who were.

Novartis's Data Reinforces Age-Appropriate Development With Zolgensma Gene Therapy Study

Basel, March 13, 2022 — Novartis today announced new data that reinforce the transformational benefit of Zolgensma® (onasemnogene abeparvovec), an essential one-time treatment for spinal muscular atrophy (SMA). The completed Phase 3 SPR1NT study demonstrated that children with three copies of the SMN2 back-up gene who were treated presymptomatically achieved age-appropriate motor milestones, including standing and walking.2 In addition, a descriptive post-hoc analyses of START, STR1VE-EU and STR1VE-US (n=65) indicated children with SMA Type 1 achieved or maintained important measures of bulbar function following treatment with Zolgensma, including ability to speak; swallow and meet nutritional needs; and maintain airway protection.3 These data are among a Zolgensma data set being presented during the 2022 Muscular Dystrophy Association (MDA) Clinical and Scientific Conference, which also include, in part, real-world data from the RESTORE registry and a chart review of US patients who changed therapy to Zolgensma.

Novartis data again demonstrate age-appropriate development when Zolgensma is used presymptomatically, and post-hoc data reveal SMA Type 1 patients could speak, swallow and maintain airway protection

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Voyager (VYGR) stock rises on the license option agreement with Novartis to get a target-specific access to next-generation TRACER AAV capsids for gene therapy programs.

Voyager (VYGR) Gains on Deal With Novartis for Gene Therapies

Voyager Therapeutics Inc.'s VYGR, +6.22% stock gained 16.8% in premarket trading on Tuesday after the gene therapy company said it inked a deal with Novartis [n: nvs] worth up to $1.7 billion. Novartis will pay $54 million upfront to license Voyager's novel adeno-associated virus (AAV) capsids for use with the gene therapies it's developing.

Voyager, Novartis sign deal worth up to $1.7 billion

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Novartis AG (NYSE: NVS) has entered a license option agreement with Voyager Therapeutics Inc (NASDAQ: VYGR) for three capsids to use in potential gene therapies for neurological diseases, with an option to access capsids for two other targets. Data suggest that AAV capsids.

Voyager Therapeutics Shares Jump On Novartis Option Agreement For Gene Therapy Programs

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Molecular Partners AG MOLN and its partner Novartis AG NVS, have requested FDA Emergency Use Authorization (EUA) for ensovibep, a DARPin antiviral therapeutic candidate to treat COVID-19. Get the Inside Access Traders Are Using to Profit More and Win Bigger.

Molecular Partners, Novartis Submit Emergency Use Authorization Request For Ensovibep For COVID-19

With the proceeds from the sale of its Roche shares and its strong Free Cash Flow, Novartis AG repaid $23.6B of its debt in FY2021. Despite developing the world's most expensive drug, Zolgensma, NVS has not reported rewarding revenues from its Spinal Muscular Atrophy therapeutics.

Cash Rich Novartis AG Paid Off $23.6B Of Its Net Debt In FY2021

Contrarian idea after the Q4 results. Solid Q4 results.

Novartis: A Good Long-Term Pick

News for Novartis Stock (NVS)