Look Under The Hood: IYY Has 20% Upside
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Mar 04 2025
0mins
Should l Buy GH?
Source: NASDAQ.COM
ETF Analyst Target Prices: The iShares Dow Jones U.S. ETF (IYY) has an implied analyst target price of $167.74, indicating a potential upside of 20.39% from its current trading price of $139.33. Notable underlying holdings with significant upside include Liberty Global Ltd, Guardant Health Inc, and Dutch Bros Inc.
Investor Considerations: Analysts' target prices may reflect optimism or could be outdated, prompting investors to conduct further research on the validity of these targets in light of recent company and industry developments.
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Analyst Views on GH
Wall Street analysts forecast GH stock price to rise
19 Analyst Rating
18 Buy
1 Hold
0 Sell
Strong Buy
Current: 102.760
Low
105.00
Averages
124.69
High
155.00
Current: 102.760
Low
105.00
Averages
124.69
High
155.00
About GH
Guardant Health, Inc. is a precision oncology company focused on guarding wellness and giving every person more time free from cancer. It provides critical insights into what drives disease through its advanced blood and tissue tests, real-world data, and artificial intelligence (AI) analytics. Guardant tests help improve outcomes across all stages of care, including screening to find cancer early, monitoring for recurrence in early-stage cancer, and helping doctors select the treatment for patients with advanced cancer. For patients with advanced-stage cancer, it has developed Guardant360 laboratory developed test (LDT), and Guardant360 CDx test, a comprehensive liquid biopsy test to provide tumor mutation profiling with solid tumors and to be used as a companion diagnostic in connection with non-small cell lung cancer (NSCLC), and breast cancer. It offers other tests, including Guardant360 Tissue test, Guardant Reveal blood test, Guardant360 Response blood test and others.
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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- No-Cost Testing: All Shield tests will be provided at no cost to patients and participating organizations, a move that not only alleviates financial burdens but also promotes health equity by removing barriers to screening in underserved and underscreened communities.
- Innovative Screening Tool: The Shield test is the first blood-based screening option for colorectal cancer approved by the FDA, intended for adults aged 45 and older at average risk, offering a more convenient screening alternative designed to increase acceptance and participation rates.
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See More
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- No-Cost Screening: All Shield tests will be provided at no cost to patients and participating organizations, aiming to eliminate financial barriers, particularly in underserved and underscreened communities, reflecting the company's commitment to improving access to screening.
- Innovative Screening Tool: The Shield test is the first FDA-approved non-invasive blood-based screening tool designed for individuals aged 45 and older at average risk, offering a more convenient screening option to increase screening rates and reduce colorectal cancer-related mortality.
- Application Deadline: Interested organizations must submit their applications by midnight PST on February 17, 2026, with approval notifications sent via email on February 20, 2026, encouraging groups with strong community and health outreach capabilities to apply.
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- Drug Discovery Innovation: Recursion Pharmaceuticals leverages AI and machine learning to accelerate drug discovery, emphasizing platform scalability to reduce development time and costs, while attracting institutional interest from firms like ARK Investment Management.
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- Strategic Collaboration Expansion: The company signed a multi-year collaboration with Merck to develop companion diagnostics and market new cancer therapies using Guardant's Infinity Smart program, further solidifying its market position in precision oncology.
- FDA Approval Milestone: Guardant360 CDx received FDA approval as a companion diagnostic for Pfizer's Braftovi and Eli Lilly's Erbitux in combination chemotherapy, marking its first FDA approval in colorectal cancer, enhancing the company's competitive edge in the market.
- Optimistic Market Outlook: Although the fourth-quarter financial results for 2025 have yet to be announced, investors maintain an optimistic view of Guardant Health's future, believing that the upcoming update could serve as a catalyst for stock price appreciation, although caution is advised against rushing into purchases in the short term.
See More
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- Collaboration Agreement: The company has signed a multi-year collaboration with Merck to develop companion diagnostics and market new cancer therapies using Guardant's Infinity Smart program, further solidifying its leadership in precision oncology.
- Positive Cash Flow: In Q3 2025, Guardant's core oncology business achieved positive free cash flow ahead of schedule, with management expecting to maintain this trend throughout 2026 and beyond, indicating significant operational efficiency improvements.
- FDA Approval: Guardant360 CDx received FDA approval as a companion diagnostic for Pfizer's Braftovi, marking its first FDA certification in colorectal cancer, which, while not impacting Q4 results, lays a solid foundation for future growth.
See More
