Akari Therapeutics raises $5M for oncology development
Written by Emily J. Thompson, Senior Investment Analyst
Updated: May 01 2025
0mins
Should l Buy AKTX?
Source: Newsfilter
Akari Therapeutics PLC's stock surged by 42.95% in pre-market trading, crossing above the 5-day SMA, as the company announced a significant financing initiative.
The price movement is attributed to Akari Therapeutics issuing 12.6 million ADSs to raise approximately $5 million for its oncology development. This includes over $1 million from new investments by the company's directors and executives, indicating strong internal confidence in the company's future. Additionally, the company is converting $2.5 million of outstanding debt into warrants for 6.4 million ADSs, aimed at improving its capital structure and funding ongoing research and development.
This financing effort reflects Akari's commitment to advancing its innovative antibody-drug conjugates (ADCs) platform, which could position the company favorably in the competitive oncology market.
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Analyst Views on AKTX
Wall Street analysts forecast AKTX stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for AKTX is 3.33 USD with a low forecast of 1.00 USD and a high forecast of 7.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.
3 Analyst Rating
3 Buy
0 Hold
0 Sell
Strong Buy
Current: 0.225
Low
1.00
Averages
3.33
High
7.00
Current: 0.225
Low
1.00
Averages
3.33
High
7.00
About AKTX
Akari Therapeutics, Plc is a biotechnology company developing precision bifunctional antibody drug conjugates (ADC) for the treatment of cancer. Utilizing its ADC discovery platform, it generates bifunctional ADC candidates and optimizes them based on the desired application to target a range of cancers. Its lead candidate, AKTX-101, targets the TROP2 receptor on cancer cells, and with a proprietary linker, delivers its novel PH1 payload directly into the tumor. PH1 is a novel bifunctional payload that is designed to disrupt RNA splicing within cancer cells, inducing tumor-specific cell death while generating immunostimulatory effects and minimizing off-target toxicity. Its pipeline includes AKTX-101 and AKTX-102, a discovery-stage ADC that pairs PH1 with an undisclosed target antibody. It is pursuing research on two additional novel payloads, such as PH5 and PH6. It also has an ADC Platform for oncology and PHP-303 program for genetic disease, liver disease and inflammation.
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.
Akari Therapeutics Highlights 2025 Progress, Plans First-in-Human Trials in 2026
- Strategic Partnership: Akari Therapeutics has established a strategic manufacturing partnership with WuXi Biologics to support its clinical trial preparations for 2026, marking a significant advancement in the company's oncology drug development.
- Innovative Drug Platform: The company is leveraging its unique PH1 payload platform to develop next-generation antibody-drug conjugates (ADCs), which have demonstrated compelling preclinical efficacy and safety, potentially transforming cancer treatment paradigms.
- Clinical Trial Plans: Akari plans to initiate its First-in-Human trial by the end of 2026, aiming to validate the efficacy of its lead candidate AKTX-101, which is expected to create new growth opportunities for the company.
- Market Potential: AKTX-101 targets the Trop2 receptor on cancer cells with a proprietary linker, anticipated to significantly enhance therapeutic efficacy and potentially synergize with checkpoint inhibitors, thereby strengthening the company's competitive position in the market.
See More
Akari Therapeutics Presents ADC Platform and 2026 Strategic Priorities at Biotech Showcase
- Strategic Presentation: Akari Therapeutics' CEO Abizer Gaslightwala will present the company's antibody-drug conjugate (ADC) platform and 2026 strategic priorities at the Biotech Showcase on January 13, 2026, aiming to attract investor interest in its innovative drug development.
- Innovative Drug Development: Akari's lead candidate, AKTX-101, targets the Trop2 receptor on cancer cells with its unique PH1 payload, showing significant effects in inducing cancer cell death and activating the immune system in preclinical studies, potentially offering new hope in cancer treatment.
- Clinical Trial Plans: The company has initiated IND enabling studies for AKTX-101, with plans to start its First-In-Human trial by late 2026 or early 2027, marking a significant step in its development and market potential in oncology.
- Multipronged Target Strategy: In addition to AKTX-101, Akari is advancing AKTX-102, an ADC targeting a novel antigen highly relevant in gastrointestinal and lung cancers, showcasing the company's broad pipeline and research capabilities across multiple cancer treatment areas.
See More
Vanda Pharmaceuticals' NEREUS Receives FDA Approval, Shares Surge 17.5%
- FDA Approval: Vanda Pharmaceuticals' NEREUS (tradipitant) has received FDA approval for the prevention of motion-induced vomiting in adults, marking a significant advancement in the company's neuropharmaceutical portfolio and is expected to drive future sales growth.
- Stock Surge: Following the FDA approval announcement, Vanda's shares jumped 17.5% to $8.26 in pre-market trading, reflecting strong market confidence in the new drug's potential and likely attracting increased investor interest.
- Market Outlook: The approval of NEREUS not only opens new market opportunities for Vanda Pharmaceuticals but also enhances its market share in the competitive antiemetic drug sector, strengthening the company's long-term profitability prospects.
- Investor Confidence: This FDA approval boosts investor expectations for Vanda's future performance, potentially prompting more institutional investors to reassess their portfolios, further driving the stock price upward.
See More
Akari Therapeutics Advances Novel Antibody Drug Conjugates with Significant Achievements in 2025
- Strategic Milestones: In 2025, Akari Therapeutics made significant strides in the antibody-drug conjugate (ADC) space, particularly with its PH1 payload-based ADC designed to overcome limitations of existing therapies, thereby offering more effective treatment options for cancer patients.
- Lead Program Progress: AKTX-101 achieved notable results in 2025, especially demonstrating strong anti-tumor activity in pancreatic and prostate cancer models, which is expected to lay a solid foundation for clinical trials and enhance the company's competitiveness in cancer treatment.
- GMP Manufacturing Partnership: The collaboration with WuXi XDC marks Akari's transition from a preclinical discovery company to a clinical biotechnology player, ensuring the production of high-quality clinical products to support upcoming trials in 2026.
- Intellectual Property Enhancement: Akari filed three new patents in 2025 to protect the uniqueness of its PH1 payload, further solidifying its market position in the ADC field and providing legal safeguards for future R&D efforts.
See More
Akari Therapeutics Highlights 2025 Progress and Future Plans
- Innovative Drug Progress: In 2025, Akari Therapeutics significantly advanced its lead antibody-drug conjugate AKTX-101, demonstrating notable activity against deadly cancers like pancreatic and prostate cancer, which is expected to yield positive outcomes in clinical trials.
- Manufacturing Partnership Initiated: The partnership with global leader WuXi XDC marks the initiation of GMP production for AKTX-101, signifying Akari's transition from a preclinical discovery company to a clinical-focused biotechnology player.
- Intellectual Property Enhancement: Throughout 2025, Akari filed three new patents to protect its unique PH1 payload platform, further solidifying its competitive edge in the oncology sector.
- Future Outlook: 2026 is anticipated to be a pivotal year for Akari, with plans to submit IND applications by the end of the year and initiate Phase 1 clinical trials for AKTX-101, potentially attracting increased investor interest.
See More
Akari Initiates GMP Manufacturing for AKTX-101 Antibody-Drug Conjugate
- GMP Manufacturing Initiation: Akari Therapeutics announced the initiation of GMP manufacturing for its lead antibody-drug conjugate, AKTX-101, marking a pivotal step toward its planned Phase 1 clinical trial expected to start in late 2026 or early 2027, reflecting the company's confidence in its scientific approach.
- Innovative Drug Mechanism: AKTX-101 utilizes a proprietary PH1 payload designed to target the Trop2 receptor on cancer cells, combining direct cytotoxicity with immune activation, which could potentially offer superior therapeutic outcomes compared to existing options.
- Strategic Partnership: Akari has partnered exclusively with WuXi XDC, a global leader in ADC development and manufacturing, leveraging their integrated platform to accelerate the production of GMP-grade material, thereby enhancing the company's competitive positioning in the market.
- Upcoming Milestones: The company plans to complete GMP manufacturing to support IND submission within the next 12 months and continue validating the PH1 payload across undisclosed targets in its pipeline, which, if successful, could redefine the therapeutic landscape for antibody-drug conjugates.
See More
Akari Therapeutics Highlights 2025 Progress, Plans First-in-Human Trials in 2026
- Strategic Partnership: Akari Therapeutics has established a strategic manufacturing partnership with WuXi Biologics to support its clinical trial preparations for 2026, marking a significant advancement in the company's oncology drug development.
- Innovative Drug Platform: The company is leveraging its unique PH1 payload platform to develop next-generation antibody-drug conjugates (ADCs), which have demonstrated compelling preclinical efficacy and safety, potentially transforming cancer treatment paradigms.
- Clinical Trial Plans: Akari plans to initiate its First-in-Human trial by the end of 2026, aiming to validate the efficacy of its lead candidate AKTX-101, which is expected to create new growth opportunities for the company.
- Market Potential: AKTX-101 targets the Trop2 receptor on cancer cells with a proprietary linker, anticipated to significantly enhance therapeutic efficacy and potentially synergize with checkpoint inhibitors, thereby strengthening the company's competitive position in the market.
See More
Akari Therapeutics Presents ADC Platform and 2026 Strategic Priorities at Biotech Showcase
- Strategic Presentation: Akari Therapeutics' CEO Abizer Gaslightwala will present the company's antibody-drug conjugate (ADC) platform and 2026 strategic priorities at the Biotech Showcase on January 13, 2026, aiming to attract investor interest in its innovative drug development.
- Innovative Drug Development: Akari's lead candidate, AKTX-101, targets the Trop2 receptor on cancer cells with its unique PH1 payload, showing significant effects in inducing cancer cell death and activating the immune system in preclinical studies, potentially offering new hope in cancer treatment.
- Clinical Trial Plans: The company has initiated IND enabling studies for AKTX-101, with plans to start its First-In-Human trial by late 2026 or early 2027, marking a significant step in its development and market potential in oncology.
- Multipronged Target Strategy: In addition to AKTX-101, Akari is advancing AKTX-102, an ADC targeting a novel antigen highly relevant in gastrointestinal and lung cancers, showcasing the company's broad pipeline and research capabilities across multiple cancer treatment areas.
See More
Vanda Pharmaceuticals' NEREUS Receives FDA Approval, Shares Surge 17.5%
- FDA Approval: Vanda Pharmaceuticals' NEREUS (tradipitant) has received FDA approval for the prevention of motion-induced vomiting in adults, marking a significant advancement in the company's neuropharmaceutical portfolio and is expected to drive future sales growth.
- Stock Surge: Following the FDA approval announcement, Vanda's shares jumped 17.5% to $8.26 in pre-market trading, reflecting strong market confidence in the new drug's potential and likely attracting increased investor interest.
- Market Outlook: The approval of NEREUS not only opens new market opportunities for Vanda Pharmaceuticals but also enhances its market share in the competitive antiemetic drug sector, strengthening the company's long-term profitability prospects.
- Investor Confidence: This FDA approval boosts investor expectations for Vanda's future performance, potentially prompting more institutional investors to reassess their portfolios, further driving the stock price upward.
See More
Akari Therapeutics Advances Novel Antibody Drug Conjugates with Significant Achievements in 2025
- Strategic Milestones: In 2025, Akari Therapeutics made significant strides in the antibody-drug conjugate (ADC) space, particularly with its PH1 payload-based ADC designed to overcome limitations of existing therapies, thereby offering more effective treatment options for cancer patients.
- Lead Program Progress: AKTX-101 achieved notable results in 2025, especially demonstrating strong anti-tumor activity in pancreatic and prostate cancer models, which is expected to lay a solid foundation for clinical trials and enhance the company's competitiveness in cancer treatment.
- GMP Manufacturing Partnership: The collaboration with WuXi XDC marks Akari's transition from a preclinical discovery company to a clinical biotechnology player, ensuring the production of high-quality clinical products to support upcoming trials in 2026.
- Intellectual Property Enhancement: Akari filed three new patents in 2025 to protect the uniqueness of its PH1 payload, further solidifying its market position in the ADC field and providing legal safeguards for future R&D efforts.
See More
Akari Therapeutics Highlights 2025 Progress and Future Plans
- Innovative Drug Progress: In 2025, Akari Therapeutics significantly advanced its lead antibody-drug conjugate AKTX-101, demonstrating notable activity against deadly cancers like pancreatic and prostate cancer, which is expected to yield positive outcomes in clinical trials.
- Manufacturing Partnership Initiated: The partnership with global leader WuXi XDC marks the initiation of GMP production for AKTX-101, signifying Akari's transition from a preclinical discovery company to a clinical-focused biotechnology player.
- Intellectual Property Enhancement: Throughout 2025, Akari filed three new patents to protect its unique PH1 payload platform, further solidifying its competitive edge in the oncology sector.
- Future Outlook: 2026 is anticipated to be a pivotal year for Akari, with plans to submit IND applications by the end of the year and initiate Phase 1 clinical trials for AKTX-101, potentially attracting increased investor interest.
See More
Akari Initiates GMP Manufacturing for AKTX-101 Antibody-Drug Conjugate
- GMP Manufacturing Initiation: Akari Therapeutics announced the initiation of GMP manufacturing for its lead antibody-drug conjugate, AKTX-101, marking a pivotal step toward its planned Phase 1 clinical trial expected to start in late 2026 or early 2027, reflecting the company's confidence in its scientific approach.
- Innovative Drug Mechanism: AKTX-101 utilizes a proprietary PH1 payload designed to target the Trop2 receptor on cancer cells, combining direct cytotoxicity with immune activation, which could potentially offer superior therapeutic outcomes compared to existing options.
- Strategic Partnership: Akari has partnered exclusively with WuXi XDC, a global leader in ADC development and manufacturing, leveraging their integrated platform to accelerate the production of GMP-grade material, thereby enhancing the company's competitive positioning in the market.
- Upcoming Milestones: The company plans to complete GMP manufacturing to support IND submission within the next 12 months and continue validating the PH1 payload across undisclosed targets in its pipeline, which, if successful, could redefine the therapeutic landscape for antibody-drug conjugates.
See More
