Kamada Halts Phase 3 Trial for Genetic Disorder, Reaffirms Future Projections
Trial Discontinuation: Kamada Ltd. has announced the discontinuation of its Phase 3 InnovAATe trial for Inhaled AAT aimed at treating Alpha-1 Antitrypsin Deficiency (AATD) due to low likelihood of demonstrating significant efficacy in improving lung function.
Stock Impact: Following the announcement, Kamada's stock experienced a decline of 5.51%, reflecting bearish market sentiment.
Future Outlook: Despite the trial setback, Kamada's CEO expressed confidence in the company's growth prospects, reiterating revenue guidance for 2025 and projecting double-digit growth in revenues and profitability for 2026.
Business Development Focus: Kamada plans to leverage its strong cash position to pursue new business development opportunities while continuing to expand its commercial portfolio, which includes FDA-approved products and a growing biosimilar portfolio.
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- 2026 Financial Outlook: Kamada projects revenues of $200 million to $205 million for 2026, representing a 13% year-over-year increase based on the midpoint of 2025 guidance, highlighting the company's ongoing organic growth potential across its diverse product portfolio in the biopharmaceutical sector.
- Adjusted EBITDA Growth: The company anticipates adjusted EBITDA to reach $50 million to $53 million in 2026, reflecting a 23% increase from the midpoint of 2025, which signifies a substantial enhancement in profitability and boosts investor confidence.
- Strong Cash Position: Kamada expects to end 2025 with approximately $75 million in cash, ensuring financial flexibility for future investments and business expansions, thereby strengthening its competitive edge in global markets.
- Strategic Development Focus: The company will continue to prioritize new business development and M&A transactions to accelerate long-term profitable growth, a strategy that will enrich its marketed product portfolio and generate synergies with existing operations.
- Contract Extension: Kamada has been awarded an extension of its existing supply tender from Canadian Blood Services for four specialty plasma-derived products, ensuring annual sales of approximately $5-$7 million between Q2-26 and Q1-28, thereby securing its market position in Canada.
- Revenue Guidance Reaffirmed: The company reiterated its full-year 2025 revenue guidance of $178 million to $182 million and adjusted EBITDA of $40 million to $44 million, reflecting strong and consistent performance in the market.
- Growth Outlook: Kamada projects double-digit growth in revenues and profitability in 2026, driven by its robust commercial portfolio and expansion of its biosimilar offerings, indicating strong competitive positioning in future markets.
- Strategic Development: The company intends to pursue additional contracts in key strategic territories, leveraging its strong cash position and existing commercial infrastructure to drive long-term growth and enhance its international market presence.

- Contract Extension: Kamada has secured an extension of its existing supply tender from Canadian Blood Services, ensuring annual sales of approximately $5-$7 million between Q2-26 and Q1-28, thereby reinforcing its leadership position in the Canadian market.
- Revenue Guidance Reaffirmed: The company reiterated its full-year 2025 revenue guidance of $178 million to $182 million and adjusted EBITDA guidance of $40 million to $44 million, reflecting strong confidence in future performance.
- Growth Outlook: Kamada projects double-digit growth in revenues and profitability in 2026, driven by a robust commercial portfolio and expansion of its biosimilar offerings, indicating significant commercial potential in international markets.
- Strategic Development: The company plans to enhance revenue growth through the expansion of normal source plasma sales and collection operations, showcasing its long-term growth strategy in the biopharmaceutical sector.
Trial Discontinuation: Kamada Ltd. has announced the discontinuation of its Phase 3 InnovAATe trial for Inhaled AAT aimed at treating Alpha-1 Antitrypsin Deficiency (AATD) due to low likelihood of demonstrating significant efficacy in improving lung function.
Stock Impact: Following the announcement, Kamada's stock experienced a decline of 5.51%, reflecting bearish market sentiment.
Future Outlook: Despite the trial setback, Kamada's CEO expressed confidence in the company's growth prospects, reiterating revenue guidance for 2025 and projecting double-digit growth in revenues and profitability for 2026.
Business Development Focus: Kamada plans to leverage its strong cash position to pursue new business development opportunities while continuing to expand its commercial portfolio, which includes FDA-approved products and a growing biosimilar portfolio.

- Trial Discontinuation: Kamada announced the discontinuation of its inhaled AAT trial based on an independent Data and Safety Monitoring Board's interim futility analysis, indicating a low likelihood of achieving statistical significance in the primary endpoint, although no safety concerns were identified.
- Revenue Guidance Reaffirmed: The company reiterated its full-year 2025 revenue guidance of $178 million to $182 million, indicating confidence in maintaining strong performance despite the disappointing trial results.
- Future Growth Outlook: Kamada projects double-digit growth in revenues and profitability for 2026, driven by its six FDA-approved specialty plasma-derived products marketed in over 30 countries and an expanding biosimilar portfolio.
- Business Development Strategy: The company is focused on pursuing new business development opportunities to support long-term growth, leveraging its strong cash position and existing commercial infrastructure to drive future market expansion and product development.








