Analysis of Weight Loss Drug Market Prospects
Written by Emily J. Thompson, Senior Investment Analyst
Updated: 1 hour ago
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Should l Buy NVO?
Source: Fool
- Challenges for Altimmune: Altimmune's leading candidate pemvidutide showed reasonable efficacy in a 2023 phase 2 trial, but high patient discontinuation rates due to adverse reactions highlight the risks and uncertainties it faces in the weight loss drug market.
- FDA Breakthrough Therapy Designation: Despite mixed phase 2 data in MASH, pemvidutide received Breakthrough Therapy designation from the FDA, indicating its potential in high unmet need areas; if it successfully passes phase 3 trials, it could significantly enhance Altimmune's market value.
- Novo Nordisk's Market Position: Facing competition from Eli Lilly, Novo Nordisk has lowered its sales guidance, yet with the approval of Wegovy and the launch of a new oral GLP-1 drug, it is poised for recovery in the coming years, demonstrating a stronger market outlook.
- Investor Outlook: 2026 is seen as a transition year for Novo Nordisk; although sales may decline this year, the anticipated impact of new approvals and label expansions is expected to gradually boost revenue, showcasing its long-term investment value in the weight loss drug market.
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Analyst Views on NVO
Wall Street analysts forecast NVO stock price to rise
8 Analyst Rating
4 Buy
3 Hold
1 Sell
Moderate Buy
Current: 38.160
Low
42.00
Averages
54.67
High
70.00
Current: 38.160
Low
42.00
Averages
54.67
High
70.00
About NVO
Novo Nordisk A/S is a global healthcare company engaged in diabetes care. The Company is also engaged in the discovery, development, manufacturing and marketing of pharmaceutical products. The Company operates through two business segments: diabetes and obesity care, and biopharmaceuticals. The Company's diabetes and obesity care segment covers insulin, GLP-1, other protein-related products, such as glucagon, protein-related delivery systems and needles, and oral anti-diabetic drugs. The Company's biopharmaceuticals segment covers the therapy areas of hemophilia care, growth hormone therapy and hormone replacement therapy. The Company also offers Saxenda product to treat obesity. It offers a range of products, including NovoLog/NovoRapid; NovoLog Mix/NovoMix; Prandin/NovoNorm; NovoSeven; Norditropin, and Vagifem. As of December 31, 2016, it marketed its products in over 180 countries. Its regional structure consists of two commercial units: North America and International Operations.
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.
- Clinical Trial Results: UBT251's phase 2 trial in China demonstrated a statistically significant mean weight loss of up to 19.7% after 24 weeks, providing new hope for obesity treatment.
- Collaborative Development: UBT251 is jointly developed by United Laboratories' wholly owned subsidiary United Biotechnology and Novo Nordisk, with the latter handling global development outside of China, reflecting a strategic partnership in obesity treatment.
- Safety Profile: The trial results indicated that UBT251 has a safe and well-tolerated profile consistent with incretin-based therapies, enhancing its competitive edge in the market.
- Market Reaction: Following a 15% drop in Novo Nordisk's stock due to CagriSema's underperformance against competitors, the positive results from UBT251 may help restore market confidence in the company's product pipeline.
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- Capital Raise Size: Novo Resources Corp aims to raise approximately C$5.8 million (around A$6 million) through the issuance of up to 59,100,000 units, demonstrating the company's confidence in future growth by supporting gold exploration in Pilbara and Victoria.
- Investor Structure: The placement targets institutional, professional, and sophisticated investors, with Canadian investors purchasing units at C$0.10 per share, while other investors outside Canada will acquire CDIs at A$0.105, reflecting the company's strategic flexibility in addressing different markets.
- Pricing Discount: The unit price represents a roughly 25% discount to the 5-day VWAP on the Toronto Stock Exchange, while the CDI price shows a 19.2% discount to the last ASX closing price, providing an attractive entry point for investors and potentially facilitating rapid capital inflow.
- Use of Proceeds: The funds raised will be allocated to drilling and reconnaissance activities in Pilbara and ongoing exploration at the Belltopper Gold Project in Victoria, aiming to enhance the company's competitiveness in the gold market and drive long-term growth.
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- Challenges for Altimmune: Altimmune's leading candidate pemvidutide showed reasonable efficacy in a 2023 phase 2 trial, but high patient discontinuation rates due to adverse reactions highlight the risks and uncertainties it faces in the weight loss drug market.
- FDA Breakthrough Therapy Designation: Despite mixed phase 2 data in MASH, pemvidutide received Breakthrough Therapy designation from the FDA, indicating its potential in high unmet need areas; if it successfully passes phase 3 trials, it could significantly enhance Altimmune's market value.
- Novo Nordisk's Market Position: Facing competition from Eli Lilly, Novo Nordisk has lowered its sales guidance, yet with the approval of Wegovy and the launch of a new oral GLP-1 drug, it is poised for recovery in the coming years, demonstrating a stronger market outlook.
- Investor Outlook: 2026 is seen as a transition year for Novo Nordisk; although sales may decline this year, the anticipated impact of new approvals and label expansions is expected to gradually boost revenue, showcasing its long-term investment value in the weight loss drug market.
See More
- Significant Stock Decline: Novo Nordisk's shares plummeted 20% this week, with a current market cap of $129 billion, primarily due to poor trial results for its new weight-loss drug CagriSema against Eli Lilly's Zepbound, undermining investor confidence.
- Intensifying Competition: Over the past three years, Eli Lilly's revenue surged by 135%, while Novo Nordisk's growth stagnated at 77%, indicating a weakening competitive position in the weight-loss drug market and a serious threat to its market share.
- Price Cut Pressures: The company announced further price cuts for its weight-loss drug Wegovy in 2027, with potential reductions of up to 50%, which could significantly impact future revenues and increase market uncertainty.
- Investor Confidence Shaken: Although Novo Nordisk's P/E ratio is approaching 10, lower than Eli Lilly's, investor concerns over market share losses and price cuts have led to perceptions of the stock as a poor investment, likely resulting in further sell-offs.
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- Securities Fraud Investigation: Pomerantz LLP is investigating whether Novo Nordisk and its executives engaged in securities fraud or other unlawful business practices, which could lead to significant losses for investors.
- Clinical Trial Failure: On February 23, 2026, Novo Nordisk announced that its experimental drug CagriSema failed to meet its primary endpoint of demonstrating non-inferiority in weight loss compared to Eli Lilly's rival drug tirzepatide, raising concerns about its efficacy.
- Stock Price Plunge: Following the disappointing trial results, Novo Nordisk's American Depositary Receipt (ADR) fell by $7.79, or 16.43%, closing at $39.63 on February 23, indicating market skepticism regarding its future prospects.
- Potential Legal Consequences: The investigation could lead to class action lawsuits against Novo Nordisk, and if wrongdoing is confirmed, it may have profound implications for the company's reputation and financial health.
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- Trial Results: Eli Lilly's oral GLP-1 medication orforglipron outperformed Novo Nordisk's oral semaglutide in the ACHIEVE-3 trial, achieving a 2.2% reduction in A1C compared to 1.4% for semaglutide, indicating a significant efficacy difference.
- Weight Loss Impact: Participants using orforglipron lost an average of 19.7 lbs (9.2%), which is 73.6% greater than the weight loss observed with semaglutide, highlighting the drug's potential in weight management.
- Regulatory Submission Progress: Lilly has submitted orforglipron for regulatory approval in over 40 countries, with a potential U.S. decision for obesity treatment expected in the second quarter of 2026, indicating a promising market outlook.
- Market Reaction Analysis: Despite a broader market decline, Eli Lilly's stock shows resilience, trading at $1008.53, which is 5.2% and 8.4% below its 20-day and 100-day simple moving averages, reflecting short-term market pressures.
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