PID's Holdings Imply 14% Gain Potential
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Nov 27 2024
0mins
Source: NASDAQ.COM
Invesco International Dividend Achievers ETF Analysis: The Invesco International Dividend Achievers ETF (PID) has an implied analyst target price of $21.89 per unit, indicating a potential upside of 14.36% from its recent trading price of $19.14.
Notable Holdings and Analyst Targets: Key holdings such as National Grid plc, Restaurant Brands International Inc, and Novartis AG show significant upside potential, with target prices suggesting increases of 28.92%, 20.28%, and 19.45% respectively compared to their current share prices.
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Analyst Views on NVS
Wall Street analysts forecast NVS stock price to fall
6 Analyst Rating
1 Buy
4 Hold
1 Sell
Hold
Current: 154.140
Low
112.00
Averages
127.75
High
143.00
Current: 154.140
Low
112.00
Averages
127.75
High
143.00
About NVS
Novartis AG is a Switzerland-based pharmaceutical company. The Company develops, manufactures, and markets branded and generic prescription drugs, active pharmaceutical ingredients (APIs), biosimilars and ophthalmic products. The Company uses science and digital technologies for treatments in the disease areas of immunology, dermatology, cancer, ophthalmology, neuroscience, respiratory, cardiovascular, renal and metabolism. The business activities of the Company are divided into two segments: Innovative Medicines, which includes innovative patent-protected prescription medicines for blood pressure, cancer and other ailments, and Sandoz, which includes generic pharmaceuticals and biosimilars.
About the author

Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
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- Gene Therapy Approval: Novartis' gene therapy Itvisma has been approved by the European Commission for children aged two and older with spinal muscular atrophy (SMA), marking its availability across all 27 EU member states as well as Norway, Iceland, and Liechtenstein.
- Innovative Treatment Option: Itvisma is the first approved gene replacement therapy targeting a broad group of SMA patients, designed to replace the survival motor neuron 1 (SMN1) gene, thereby enhancing Novartis' product offerings in the SMA treatment landscape.
- Market Competitive Edge: Together with the existing Zolgensma therapy, Itvisma provides gene replacement therapy options for SMA patients at various stages, from newborns to adults, significantly strengthening Novartis' competitive position in the European market.
- Clinical Research Backing: The approval follows the pivotal STEER study results, which demonstrated Itvisma's statistically significant improvement on SMA disease progression scales, further solidifying Novartis' leadership in muscle disease therapies.
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- Gene Therapy Approval: Novartis's Itvisma gene therapy has received approval from the European Commission, specifically designed for treating patients with 5q spinal muscular atrophy, marking a significant advancement in the rare disease sector and expected to enhance the company's competitive position in this market.
- Successful Clinical Trials: Itvisma demonstrated impressive results in the STEER clinical program, with both the Phase 1/2 STRONG trial and Phase 3b STRENGTH trial showing significant efficacy, as treated subjects exhibited an average improvement of 2.39 points on the Hammerstein Functional Motor Scale, indicating the therapy's effectiveness and sustainability.
- Market Exclusivity: Itvisma is now the only approved gene therapy for adults with SMA in the European Union, further solidifying Novartis's leadership in the gene therapy space while providing a new revenue stream for the company.
- Competitive Product Scrutiny: Novartis's other drug, Zolgensma, is under review due to liver-related side effects in infants, which clarifies Itvisma's market outlook and may attract more patients to choose this therapy.
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