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.

The CHMP gives a positive opinion on, and recommends approval for Novartis' (NVS) Tabrecta for treating patients with METex14 advanced non-small cell lung cancer.

Novartis (NVS) Gets Positive CHMP Opinion on Lung Cancer Drug

Big pharma company Novartis pays big dividends -- but there are other reasons for investors to buy its stock.

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Basel, April 22, 2022 — Novartis announced today that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion and recommended granting marketing authorization of Tabrecta® (capmatinib) as a monotherapy for the treatment of adults with advanced non-small cell lung cancer (NSCLC) harboring alterations leading to mesenchymal-epithelial-transition factor gene (MET) exon 14 (METex14) skipping who require systemic therapy following prior treatment with immunotherapy and/or platinum-based chemotherapy.

Novartis receives positive CHMP opinion for Tabrecta® for patients with METex14 advanced non-small cell lung cancer

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Swiss drugmaker Novartis will cut thousands of jobs worldwide as it combines its pharma and oncology businesses in a reorganisation announced last week, Swiss newspaper Tages-Anzeiger reported on Tuesday, citing unnamed company sources.

Novartis to cut thousands of jobs in global revamp - paper

Novartis (NVS) application seeking approval of tislelizumab in multiple non-small cell lung cancer and esophageal squamous cell carcinoma indications gets EMA's validation.

Novartis (NVS) Anti-PD-1 Drug Validated by EMA for Lung Cancer

The FDA approves Novartis' (NVS) Vijoice (alpelisib) for the treatment of select patients with PIK3CA-related overgrowth spectrum.

Novartis (NVS) Gets FDA Nod for Vijoice in Rare Disorder

Basel, April 6 , 2022 — Novartis today announced that the U.S. Food and Drug Administration (FDA) granted accelerated approval to Vijoice® (alpelisib) for the treatment of adult and pediatric patients 2 years of age and older with severe manifestations of PIK3CA-Related Overgrowth Spectrum (PROS) who require systemic therapy.1 Vijoice is the first FDA-approved treatment for PROS, a spectrum of rare conditions characterized by overgrowths and blood vessel anomalies impacting an estimated 14 people per million.2,3 In accordance with the Accelerated Approval Program, continued approval may be contingent upon verification and description of clinical benefit from confirmatory evidence.

FDA approves Novartis Vijoice® (alpelisib) as first and only treatment for select patients with PIK3CA-Related Overgrowth Spectrum (PROS)

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The bond market is starting to signal that a recession and bear market could be coming in 2023 or 2024.

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Novartis ( NVS , Financial) investors hope the organizational changes the company is making can shake loose some shareholder value. Since February 2020, Novartis stock has dropped nearly 12% while the Invesco Dynamic Pharmaceuticals ETF ( PJP , Financial) has climbed more than 25%.

Changes at Novartis Aimed at Boosting Shareholder Value

The reorganization is the latest move from Vas Narasimhan, who took over the Swiss drugmaker in 2018.

Novartis CEO Continues His Shake-Up, Says It Will Save More Than $1 Billion Annually

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

News for Novartis Stock (NVS)