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Akari Therapeutics to Participate in the Corporate Connect Webinar Series Virtual Conference Hosted by Webull Financial

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Akari Therapeutics (Nasdaq: AKTX) will present a live video webcast on Tuesday, February 10, 2026 at 1:00 PM EST as part of Webull Financial’s Corporate Connect Webinar Series.

CEO Abizer Gaslightwala will provide a corporate overview of Akari’s ADC platform, the proprietary PH1 spliceosome‑modulating payload, lead program AKTX‑101 (Trop2‑targeting ADC), IND‑enabling activities toward a first‑in‑human trial in late 2026 or early 2027, and a brief update on AKTX‑102.

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News Market Reaction

-2.22%
5 alerts
-2.22% News Effect
-4.0% Trough in 12 hr 41 min
-$258K Valuation Impact
$11M Market Cap
0.7x Rel. Volume

On the day this news was published, AKTX declined 2.22%, reflecting a moderate negative market reaction. Argus tracked a trough of -4.0% from its starting point during tracking. Our momentum scanner triggered 5 alerts that day, indicating moderate trading interest and price volatility. This price movement removed approximately $258K from the company's valuation, bringing the market cap to $11M at that time.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

Webinar date: February 10–11, 2026 Presentation time: 1:00 PM EST FIH timing goal: Late 2026 or early 2027
3 metrics
Webinar date February 10–11, 2026 Corporate Connect Webinar Series virtual conference
Presentation time 1:00 PM EST Live video webcast on Tuesday, February 10, 2026
FIH timing goal Late 2026 or early 2027 Target start for first-in-human trial of AKTX-101

Market Reality Check

Price: $0.2350 Vol: Volume 225,993 is below t...
low vol
$0.2350 Last Close
Volume Volume 225,993 is below the 20-day average of 365,154, suggesting limited pre-event positioning. low
Technical Shares at $0.2301 are trading below the 200-day MA of $0.84, reflecting a longer-term downtrend.

Peers on Argus

While AKTX trades near its 52-week low with a -1.33% move, several close biotech...
1 Up

While AKTX trades near its 52-week low with a -1.33% move, several close biotech peers like QTTB, RNTX, KZR, LIXT, and ALLR also show single-day declines ranging from about -1% to nearly -7%, pointing to generally weak sentiment in neighboring names but no clear coordinated sector rotation.

Historical Context

5 past events · Latest: Jan 26 (Positive)
Pattern 5 events
Date Event Sentiment Move Catalyst
Jan 26 Patent and pipeline Positive -0.5% Filed provisional patent for AKTX-102 and reiterated PH1 ADC platform plans.
Jan 09 CEO strategic update Positive -0.3% CEO outlined 2025 progress and steps toward clinical transition in 2026.
Jan 08 Conference presentation Positive -1.7% Announced Biotech Showcase presentation on ADC platform and 2026 milestones.
Dec 30 Year-end shareholder letter Positive +2.3% Year-end letter detailed PH1 payload progress and Phase 1 timing goals.
Dec 23 GMP manufacturing start Positive -7.1% Initiated GMP manufacturing of AKTX-101 to support first-in-human trial.
Pattern Detected

Recent positive corporate and pipeline updates have often coincided with flat to negative next-day price reactions, suggesting a pattern of selling or indifference into news.

Recent Company History

Over the past months, Akari has consistently highlighted progress on its ADC platform and PH1 spliceosome-modulating payload. Updates included initiating GMP manufacturing for AKTX-101, outlining a path to a Phase 1 first-in-human trial in late 2026 or early 2027, and filing a provisional patent for AKTX-102. Multiple investor-focused communications and conference presentations emphasized the oncology repositioning. Despite this, several announcements saw negative or muted one-day price reactions, framing today’s webinar news within a trend of cautious market response.

Regulatory & Risk Context

Active S-3 Shelf
Shelf Active
Active S-3 Shelf Registration 2025-07-29

Akari has an effective S-3 shelf registration filed on 2025-07-29 with recorded usage via at least 2 prospectus supplements, including the 2025-12-17 424B5 offering. Shelf data show remaining capacity of $72,500,000 against cumulative usage of $2,500,000, indicating substantial room for additional registered financings.

Market Pulse Summary

This announcement centers on an investor-focused webinar where management plans to highlight Akari’s...
Analysis

This announcement centers on an investor-focused webinar where management plans to highlight Akari’s ADC platform, PH1 spliceosome-modulating payload, and lead program AKTX-101 with first-in-human studies targeted for late 2026 or early 2027. Recent history shows multiple communications about patents, manufacturing and strategy as the company transitions toward clinical development. Investors may watch for consistency with prior timelines and any additional clarity on development milestones or financing plans disclosed during the presentation.

Key Terms

antibody drug conjugates, adcs, rna-splicing, spliceosome-modulating, +3 more
7 terms
antibody drug conjugates medical
"an oncology biotechnology company pioneering next-generation antibody drug conjugates (ADCs)"
Antibody drug conjugates are targeted medicines that combine an antibody, which seeks out specific markers on diseased cells, with a powerful drug that is released only when the antibody binds its target. Think of it as a guided missile that delivers a toxic payload directly to its target, reducing damage to healthy cells; investors watch them because successful ADCs can offer high-value, niche treatments and drive strong revenue and patent-based protection for developers.
adcs medical
"next-generation antibody drug conjugates (ADCs) powered by novel RNA-splicing payloads"
Antibody-drug conjugates (ADCs) are targeted cancer medicines that combine an antibody, which seeks out specific markers on tumor cells, with a powerful drug payload that is released once the antibody binds its target. Think of them as a guided missile that delivers a toxic package directly to diseased cells to limit harm to healthy tissue. Investors watch ADC news closely because clinical trial results, manufacturing complexity and regulatory decisions can sharply change a biotech company’s value.
rna-splicing medical
"next-generation antibody drug conjugates (ADCs) powered by novel RNA-splicing payloads"
RNA splicing is the cellular process that edits raw genetic messages (RNA) by cutting out noncoding sections and joining the remaining pieces so a usable blueprint for a protein is produced. It matters to investors because changes in splicing can create different protein versions that drive disease, serve as drug targets, or act as biomarkers; therapies that modify splicing can therefore create new treatment opportunities or risks for biotech investments.
spliceosome-modulating medical
"proprietary PH1 spliceosome-modulating payload"
Spliceosome-modulating describes drugs or therapies that alter the spliceosome, the cell’s machinery that cuts and joins pieces of messenger RNA before it becomes a protein. Like changing how a film editor cuts scenes, these treatments can change which protein versions a cell makes, potentially correcting genetic errors or blocking cancer growth. For investors, this signals a high-science approach with the potential for big clinical gains but also greater development risk and dependence on precise patient selection.
trop2 medical
"AKTX-101, a Trop2-targeting ADC designed to deliver PH1"
Trop2 is a protein found on the surface of many cancer cells that acts like a visible flag doctors and drugmakers can use to find and attack tumors. It matters to investors because drugs designed to bind Trop2 can deliver treatment directly to cancer cells, affecting how well a therapy works, which patients it helps, and the potential market and regulatory value of companies developing those targeted treatments.
ind-enabling regulatory
"ongoing IND-enabling activities targeting a first-in-human trial"
Ind-enabling describes the preclinical tests and safety work a drug candidate must pass before a company can ask regulators for permission to start human trials (an Investigational New Drug or IND filing). Think of it as the mechanical inspection and crash-testing a prototype car needs before it can legally be driven on public roads; for investors, successful ind-enabling work reduces technical and regulatory risk and makes clinical progress and potential value creation more likely.
first-in-human medical
"targeting a first-in-human trial in late 2026 or early 2027"
A first-in-human study is the initial test of a new drug, medical device, or therapy in people to check safety, side effects and appropriate dosing. It matters to investors because it marks a major development milestone: successful early human testing can reduce scientific and regulatory uncertainty, much like moving a prototype from the workshop to a real-world test drive, and often affects a company’s valuation and funding prospects.

AI-generated analysis. Not financial advice.

– Live video webcast on Tuesday, February 10th at 1:00 PM EST

TAMPA, Fla. and LONDON, Feb. 05, 2026 (GLOBE NEWSWIRE) -- Akari Therapeutics, Plc (Nasdaq: AKTX), an oncology biotechnology company pioneering next-generation antibody drug conjugates (ADCs) powered by novel RNA-splicing payloads, today announced that it will participate in the Corporate Connect Webinar Series hosted by Webull Financial being held virtually February 10-11, 2026.

As part of the presentation, Abizer Gaslightwala, Director, President and CEO of Akari Therapeutics, will provide a corporate overview highlighting the Company’s next-generation antibody drug conjugate platform and proprietary PH1 spliceosome-modulating payload. He will discuss Akari’s lead program, AKTX-101, a Trop2-targeting ADC designed to deliver PH1 directly to tumors with limited off-target effects, as well as ongoing IND-enabling activities targeting a first-in-human trial in late 2026 or early 2027. Mr. Gaslightwala will also provide a brief update on AKTX-102, an additional ADC program focused on GI and lung cancers.

Details of the presentation are as follows: 

Date and Time: Tuesday, February 10, 2026 at 1:00 PM EST
Presenter: Abizer Gaslightwala, Director, President and CEO of Akari
Registration Link: Here 

About Webull Financial  

Webull Financial is a leading online brokerage platform committed to empowering self-directed investors with innovative tools and cutting-edge technology. With low-cost trading on a wide range of assets, advanced charting tools, and real-time market data, Webull is revolutionizing the way individuals approach investing. The user-centric approach and commitment to staying at the forefront of industry trends underscore the mission to provide a seamless and rewarding experience for traders of all levels. Through the Webull Group, Webull Financial and its affiliates combine to serve tens of millions of users from over 180 countries worldwide. Securities and futures trading is offered to customers by Webull Financial LLC ("Webull Financial"), a broker-dealer registered with the Securities and Exchange Commission (SEC) and a futures commission merchant registered with the Commodity Futures Trading Commission (CFTC). Webull Financial is a member of the Financial Industry Authority (FINRA), the National Futures Association (NFA), and the Securities Investor Protection Corporation (SIPC). All investing is subject to risk, including the possible loss of principal. For more information about Webull, visit www.webull.com

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 and 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 tubulin 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 system to drive robust and durable activity. In preclinical studies, AKTX-101 has 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 late 2026/early 2027, and is also advancing AKTX-102, an ADC against a novel target highly relevant in GI and lung cancers. 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 any other diseases, and ultimately bring therapies to patients. 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
AKTX@jtcir.com


FAQ

When is Akari Therapeutics (AKTX) presenting at the Webull Corporate Connect Webinar?

Akari Therapeutics will present on Tuesday, February 10, 2026 at 1:00 PM EST. According to Akari Therapeutics, the presentation is a live video webcast as part of Webull Financial’s Corporate Connect Webinar Series running February 10–11, 2026.

What will Akari Therapeutics CEO Abizer Gaslightwala discuss during the AKTX presentation?

He will provide a corporate overview of the company’s ADC platform and PH1 payload. According to Akari Therapeutics, topics include lead program AKTX‑101, IND‑enabling activities, timing for first‑in‑human trial, and a brief AKTX‑102 update.

What is AKTX‑101 and what clinical timeline did Akari (AKTX) disclose?

AKTX‑101 is a Trop2‑targeting ADC designed to deliver PH1 directly to tumors with limited off‑target effects. According to Akari Therapeutics, IND‑enabling work is underway aiming for a first‑in‑human trial in late 2026 or early 2027.

Will Akari Therapeutics offer updates on other programs besides AKTX‑101 during the Feb 10 webcast?

Yes, the company will provide a brief update on AKTX‑102, an ADC program focused on gastrointestinal and lung cancers. According to Akari Therapeutics, AKTX‑102 update will be part of the CEO’s presentation.

How can investors access Akari Therapeutics’ (AKTX) Webull webinar presentation on February 10, 2026?

Investors can join the live video webcast on February 10, 2026 at 1:00 PM EST via the registration link provided for the event. According to Akari Therapeutics, registration is available through the Webull Corporate Connect Webinar Series page.
Akari Therapeutics Plc

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Biotechnology
Pharmaceutical Preparations
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United States
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