Biotech Stocks with High Growth Potential
Written by Emily J. Thompson, Senior Investment Analyst
Updated: 18 hours ago
0mins
Should l Buy CRSP?
Source: Fool
- CRISPR Breakthrough: CRISPR Therapeutics received approval for its first gene editing treatment, Casgevy, in 2023, marking a significant milestone as the world's first CRISPR therapy, generating $116 million in revenue in 2022, with expectations for a 58% stock price increase over the next 12 months.
- Clinical Trial Progress: The company anticipates releasing results from various clinical trials, including zugo-cel for autoimmune diseases and CTX310 for heart disease, which could bolster market confidence and potentially elevate stock prices.
- Viking's Promising Therapy: Viking Therapeutics is advancing VK2735 through late-stage clinical trials, with both injectable and oral forms expected to enter the market, targeting the nearly $100 billion obesity drug market, with analysts predicting a potential 200% stock price increase.
- Significant Market Potential: As GLP-1 drugs gain popularity, Viking's VK2735 is poised to capture substantial market share amid rising global demand for weight loss medications, offering early investors the prospect of substantial returns.
Trade with 70% Backtested Accuracy
Stop guessing "Should I Buy CRSP?" and start using high-conviction signals backed by rigorous historical data.
Sign up today to access powerful investing tools and make smarter, data-driven decisions.
Analyst Views on CRSP
Wall Street analysts forecast CRSP stock price to rise
10 Analyst Rating
8 Buy
2 Hold
0 Sell
Strong Buy
Current: 54.640
Low
50.00
Averages
78.89
High
105.00
Current: 54.640
Low
50.00
Averages
78.89
High
105.00
About CRSP
CRISPR Therapeutics AG is a Switzerland-based gene editing company focused on the development of CRISPR/Cas9-based therapeutics. CRISPR/Cas9 stands for Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) and is a technology for gene editing, the process of precisely altering specific sequences of genomic DNA. The Company aims to apply this technology to disrupt, delete, correct and insert genes to treat genetically-defined diseases and to engineer advanced cellular therapies. The Company has acquired the rights to the intellectual property (IP) encompassing CRISPR/Cas9 and related technologies and is also involved in its own IP research and additional in-licensing efforts. The Company product development and partnership strategies are designed to exploit the full potential of the CRISPR/Cas9 platform while maximizing the probability of successfully developing their product candidates.
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.
- Market Leadership: CRISPR Therapeutics' gene-editing therapy Casgevy, approved by the FDA in December 2023 in partnership with Vertex Pharmaceuticals, stands as the only approved CRISPR gene-editing therapy, marking the company's leading position in the gene therapy market.
- Sales Growth Potential: Although only 64 patients received Casgevy treatment in 2025, sales are projected to soar from $37.3 million in 2025 to $374.9 million by 2027, indicating strong growth potential as market education progresses.
- Rich R&D Pipeline: CRISPR Therapeutics has five therapies in clinical trials, four of which are wholly owned by the company, targeting autoimmune diseases, cardiovascular conditions, and Type 1 diabetes, showcasing a broad strategic focus in gene therapy.
- Strong Financial Position: Despite burning through $345.9 million in cash in 2025, the company retains nearly $2 billion in cash and only $188 million in long-term debt, demonstrating financial resilience for future R&D and market expansion.
See More
- Gene Editing Breakthrough: CRISPR Therapeutics' Casgevy became the first approved gene-editing therapy for rare blood diseases, marking a significant milestone; however, the company's stock has underperformed since then, yet its future potential continues to attract investor interest.
- Pipeline Prospects: The development of zugo-cel aims to treat various cancers and autoimmune diseases using healthy donor cells, addressing manufacturing limitations and immune rejection risks associated with traditional CAR-T therapies, and positive clinical data could lead to a stock price surge.
- FDA Certification Acceleration: Zugo-cel has received the Regenerative Medicine Advanced Therapy designation from the FDA, which will expedite its development and approval process, indicating its potential in treating serious diseases with high unmet needs, thereby boosting investor confidence.
- Risks and Opportunities: While CRISPR Therapeutics' clinical programs appear promising, failures in key candidates could lead to significant stock volatility, necessitating investors to carefully weigh the risks against potential rewards.
See More
- Gene Editing Breakthrough: CRISPR Therapeutics' Casgevy became the first approved gene-editing therapy for rare blood diseases, marking a significant advancement for the company, which has faced stock underperformance since then, yet its innovative potential continues to attract market interest.
- Promising Treatment Options: The company is developing zugo-cel, which aims to address manufacturing limitations of CAR-T therapies by using healthy donor cells instead of patients' own cells, thereby reducing the risk of immune rejection and enhancing its potential to treat cancers and autoimmune diseases.
- Regulatory Support: Zugo-cel has received the FDA's Regenerative Medicine Advanced Therapy (RMAT) designation, which is designed to expedite the development of treatments for serious diseases with high unmet needs, indicating strong clinical prospects for the drug.
- Diverse Pipeline: CRISPR Therapeutics' pipeline also includes candidates like CTX310, which could help lower bad cholesterol, and SRSD107, a next-generation anticoagulant, and successful clinical trials for these drugs could significantly enhance the company's market position in the biotech sector.
See More
- Sales Growth Outlook: Vertex Pharmaceuticals reported higher expected sales for Casgevy in 2025 during its fourth-quarter earnings, indicating profitability primarily from cystic fibrosis treatments, although its stock price moderated shortly after the report.
- Market Potential for CRISPR: As the developer of Casgevy, CRISPR Therapeutics stands to benefit from increased sales, and with five other candidates in clinical trials, it demonstrates strong R&D capabilities in gene editing with larger potential patient pools.
- Financial Status Review: Although CRISPR Therapeutics is not yet profitable and has seen a 64% stock price decline over the past five years, it holds over $1.9 billion in cash, allowing for increased investment in pipeline candidates if Casgevy sales grow as expected.
- High-Risk, High-Reward: CRISPR Therapeutics is viewed as a high-risk, high-reward investment; despite current losses, its potential for functional cures and existing manufacturing infrastructure make it an attractive acquisition target, with its low price presenting a buying opportunity for investors.
See More
- CRISPR Breakthrough: CRISPR Therapeutics received approval for its first gene editing treatment, Casgevy, in 2023, marking a significant milestone as the world's first CRISPR therapy, generating $116 million in revenue in 2022, with expectations for a 58% stock price increase over the next 12 months.
- Clinical Trial Progress: The company anticipates releasing results from various clinical trials, including zugo-cel for autoimmune diseases and CTX310 for heart disease, which could bolster market confidence and potentially elevate stock prices.
- Viking's Promising Therapy: Viking Therapeutics is advancing VK2735 through late-stage clinical trials, with both injectable and oral forms expected to enter the market, targeting the nearly $100 billion obesity drug market, with analysts predicting a potential 200% stock price increase.
- Significant Market Potential: As GLP-1 drugs gain popularity, Viking's VK2735 is poised to capture substantial market share amid rising global demand for weight loss medications, offering early investors the prospect of substantial returns.
See More
- Gene Editing Leader: CRISPR Therapeutics stands out as a leader in gene editing, utilizing CRISPR technology to repair specific genes for disease treatment, having secured the first-ever FDA approval for its CRISPR product, Casgevy, marking a significant breakthrough in the biotech industry.
- Massive Market Potential: The launch of Casgevy is gaining momentum, with CRISPR Therapeutics stating that the product has 'multi-billion-dollar potential'; although profits are shared with partner Vertex Pharmaceuticals, it still represents substantial growth opportunities for the company.
- Catalysts in 2026: The company expects to release clinical trial updates for cardiovascular candidate CTX310 and thromboembolic candidate CTX611 in the second half of 2026, along with trials for refractory hypertension and lung/liver disease, which could provide short-term stock support.
- Long-Term Growth Outlook: With a robust pipeline and the success of Casgevy, CRISPR Therapeutics is well-positioned for long-term growth, making it a stock that investors may regret missing out on in 2026.
See More









