Akari Therapeutics will host a live webcast with CEO Abizer Gaslightwala on May 20, discussing their ADC pipeline and therapies.
Quiver AI Summary
Akari Therapeutics, an oncology biotechnology company, announced that CEO Abizer Gaslightwala will participate in a virtual fireside chat at A.G.P.'s Annual Healthcare Company Showcase on May 20, 2026. The discussion will focus on the company's innovative antibody drug conjugate (ADC) pipeline, particularly its lead program, AKTX-101, which targets the Trop2 receptor in cancer cells using a novel RNA splicing modulator payload, PH1. This technology aims to induce cancer cell death while enhancing immune response. The company is also developing another candidate, AKTX-102, targeting CEACAM5, and has plans for further studies to advance its clinical trials. Investors can register for the event on Akari's website.
Potential Positives
- Abizer Gaslightwala, President and CEO, will present at A.G.P.’s Annual Healthcare Company Showcase, increasing visibility for Akari Therapeutics in the oncology biotechnology industry.
- The announcement highlights Akari's differentiated ADC pipeline, underscoring the potential of their proprietary PH1 RNA splicing modulator payload platform and lead program, AKTX-101.
- Preclinical studies suggest that AKTX-101 demonstrates significant activity and prolonged survival compared to traditional ADCs, positioning the company favorably in the competitive landscape of cancer treatments.
- The company is advancing its initiatives with plans to start its First-In-Human trial for AKTX-101 by mid-2027, indicating ongoing progress and commitment to development timelines.
Potential Negatives
- The company faces significant uncertainty regarding the timing of its First-In-Human trial for its lead product candidate, AKTX-101, which is projected to start by mid-2027, potentially signaling delays in its clinical development timeline.
- The press release highlights the need for additional capital, which may raise concerns about the company's financial stability and ability to fund ongoing research and development initiatives.
- Potential risks related to global political and economic conditions could impact the company’s operations and future prospects, introducing a level of instability that may deter investors.
FAQ
What is the date of the fireside chat with Abizer Gaslightwala?
The fireside chat will take place on Wednesday, May 20, 2026.
How can I register for the Akari Therapeutics event?
You can register for the event by clicking the registration link in the press release.
What is Akari Therapeutics known for developing?
Akari Therapeutics specializes in developing antibody drug conjugates (ADCs) with novel RNA splicing modulator payloads.
What is the lead product candidate of Akari Therapeutics?
The lead candidate is AKTX-101, which targets the Trop2 receptor on cancer cells.
When is the First-In-Human trial for AKTX-101 expected to start?
The First-In-Human trial for AKTX-101 is planned to begin by mid-2027.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$AKTX Hedge Fund Activity
We have seen 2 institutional investors add shares of $AKTX stock to their portfolio, and 23 decrease their positions in their most recent quarter.
Here are some of the largest recent moves:
- ARMISTICE CAPITAL, LLC removed 2,722,993 shares (-100.0%) from their portfolio in Q1 2026, for an estimated $14,023,413
- WARBERG ASSET MANAGEMENT LLC removed 308,340 shares (-100.0%) from their portfolio in Q1 2026, for an estimated $1,587,951
- PALO ALTO INVESTORS LP removed 146,024 shares (-100.0%) from their portfolio in Q1 2026, for an estimated $752,023
- HIGHTOWER ADVISORS, LLC removed 79,236 shares (-100.0%) from their portfolio in Q1 2026, for an estimated $408,065
- JANE STREET GROUP, LLC removed 71,644 shares (-100.0%) from their portfolio in Q1 2026, for an estimated $368,966
- CWA ASSET MANAGEMENT GROUP, LLC removed 55,000 shares (-100.0%) from their portfolio in Q1 2026, for an estimated $283,250
- XTX TOPCO LTD removed 49,019 shares (-100.0%) from their portfolio in Q1 2026, for an estimated $252,447
To track hedge funds' stock portfolios, check out Quiver Quantitative's institutional holdings dashboard. You can access data on hedge funds moves and 13F filings through the Quiver Quantitative API 13F endpoint.
$AKTX Price Targets
Multiple analysts have issued price targets for $AKTX recently. We have seen 2 analysts offer price targets for $AKTX in the last 6 months, with a median target of $14.0.
Here are some recent targets:
- Sean Lee from HC Wainwright & Co. set a target price of $27.0 on 04/01/2026
- Aydin Huseynov from Ladenburg Thalmann set a target price of $1.0 on 01/05/2026
Full Release
Live webcast fireside chat with Abizer Gaslightwala, President and Chief Executive Officer, on Wednesday, May 20, 2026
Register for the event
here
TAMPA, Fla. and LONDON, May 18, 2026 (GLOBE NEWSWIRE) -- Akari Therapeutics, Plc (Nasdaq: AKTX), an oncology biotechnology company developing antibody drug conjugates (ADCs) with novel RNA splicing modulator payloads, today announced that Abizer Gaslightwala, President and Chief Executive Officer of Akari Therapeutics, will participate in a fireside chat at A.G.P.’s Annual Healthcare Company Showcase being held virtually on Wednesday, May 20, 2026.
Management will discuss the Company’s differentiated ADC pipeline, including progress across its proprietary PH1 RNA splicing modulator payload platform and lead TROP2-targeting ADC program, AKTX-101.
Click here to register for the event. A live webcast of the fireside chat will be accessible on the Presentations page in the Investors section of the Company’s website.
About Akari Therapeutics
Akari Therapeutics is an oncology biotechnology company developing next-generation antibody drug conjugates (ADCs) with a unique payload, PH1, which targets RNA splicing. Utilizing its innovative ADC discovery platform, the Company has the ability to generate ADC candidates and optimize them based on the desired application to any antigen target of interest. Akari’s lead candidate, AKTX-101, targets the Trop2 receptor on cancer cells with a proprietary linker, enabling it to deliver its novel PH1 payload directly into the tumor with minimal off-target effects. Unlike current ADCs that use microtubule inhibitors and DNA-damaging agents as their payloads, PH1 is a novel payload that is a spliceosome modulator designed to disrupt RNA splicing within cancer cells. This splicing modulation has been shown in preclinical animal models to induce cancer cell death while activating both the innate and adaptive immune systems to drive robust and durable activity. In preclinical studies, AKTX-101 has been shown to have significant activity and prolonged survival relative to ADCs with traditional payloads. Additionally, AKTX-101 has the potential to be synergistic with checkpoint inhibitors and has demonstrated prolonged survival as both a single agent and in combination with checkpoint inhibitors. The PH1 payload has also been demonstrated to be very active against cancer cells with key oncogenic drivers such as KRAS, BRAF, ARV7, FGFR3 fusions, and others. The Company has initiated IND enabling studies for AKTX-101 with a goal of starting its First-In-Human trial by mid-2027. Akari is also developing AKTX-102, an ADC candidate targeting CEACAM5 (Carcinoembryonic Antigen-related Cell Adhesion Molecule-5), a well-validated tumor antigen broadly expressed across multiple solid tumors. AKTX-102 is designed to leverage Akari’s proprietary PH1 spliceosome-modulating payload and a novel antibody construct to enable differentiated tumor cell killing and immune activation.
For more information about the Company, please visit www.akaritx.com and connect on X and LinkedIn .
Cautionary Note Regarding Forward-Looking Statements
This press release includes express or implied forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, about the Company that involve risks and uncertainties relating to future events and the future performance of the Company. Actual events or results may differ materially from these forward-looking statements. Words such as “will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,” “intend,” “believe,” “estimate,” “predict,” “project,” “potential,” “continue,” “future,” “opportunity” “will likely result,” “target,” variations of such words, and similar expressions or negatives of these words are intended to identify such forward-looking statements, although not all forward-looking statements contain these identifying words. Examples of such forward-looking statements include, but are not limited to, express or implied statements regarding the ability of the Company to advance its product candidates for the treatment of cancer and the timing of commencement of a Phase I clinical trial. These statements are based on the Company’s current plans, estimates and projections. By their very nature, forward-looking statements involve inherent risks and uncertainties, both general and specific. A number of important factors, including those described in this communication, could cause actual results to differ materially from those contemplated in any forward-looking statements. Factors that may affect future results and may cause these forward-looking statements to be inaccurate include, without limitation: the Company’s need for additional capital; the potential impact of unforeseen liabilities, future capital expenditures, revenues, costs, expenses, earnings, synergies, economic performance, indebtedness, financial condition and losses on the future prospects, business and management strategies for the management, expansion and growth of the business; risks related to global as well as local political and economic conditions, including interest rate and currency exchange rate fluctuations; potential delays or failures related to research and/or development of the Company’s programs or product candidates; risks related to any loss of the Company’s patents or other intellectual property rights; any interruptions of the supply chain for raw materials or manufacturing for the Company’s product candidates, including as a result of potential tariffs; the nature, timing, cost and possible success and therapeutic applications of product candidates being developed by the Company and/or its collaborators or licensees; the extent to which the results from the research and development programs conducted by the Company, and/or its collaborators or licensees may be replicated in other studies and/or lead to advancement of product candidates to clinical trials, therapeutic applications, or regulatory approval; uncertainty of the utilization, market acceptance, and commercial success of the Company’s product candidates; risks related to competition for the Company’s product candidates; and the Company’s ability to successfully develop or commercialize its product candidates. While the foregoing list of factors presented here is considered representative, no list should be considered to be a complete statement of all potential risks and uncertainties. More detailed information about the Company and the risk factors that may affect the realization of forward-looking statements is set forth in the Company’s filings with the SEC, copies of which may be obtained from the SEC’s website at www.sec.gov. The Company assumes no, and hereby disclaims any, obligation to update the forward-looking statements contained in this press release except as required by law.
Investor Relations Contact
JTC Team, LLC
Jenene Thomas
908-824-0775
[email protected]