STOCK TITAN

iBio Appoints Distinguished Biotech Leader, Elizabeth Stoner, to its Board of Directors

Rhea-AI Impact
(Neutral)
Rhea-AI Sentiment
(Positive)
Tags
management

iBio (NASDAQ:IBIO) appointed Elizabeth Stoner, M.D., M.S., to its Board of Directors and to the Compensation Committee on May 8, 2026, concurrent with the departure of director Eef Schimmelpennink.

Dr. Stoner brings over 35 years of R&D leadership, industry and board experience and will support iBio as it begins its first human clinical trial for IBIO-610, IBIO-600 and other assets.

Loading...
Loading translation...

AI-generated analysis. Not financial advice.

Positive

  • Board addition: Elizabeth Stoner appointed as independent director
  • Experience: 35+ years in biotech R&D and global clinical development
  • Committee role: Named to the Compensation Committee
  • Clinical milestone: Support ahead of company's first human clinical trial

Negative

  • Board turnover: Eef Schimmelpennink stepped down from the board

News Market Reaction – IBIO

+4.27%
1 alert
+4.27% News Effect
+$2M Valuation Impact
$59.28M Market Cap
1.51K Volume

On the day this news was published, IBIO gained 4.27%, reflecting a moderate positive market reaction. This price movement added approximately $2M to the company's valuation, bringing the market cap to $59.28M at that time.

Data tracked by StockTitan Argus on the day of publication.

SAN DIEGO, May 08, 2026 (GLOBE NEWSWIRE) -- iBio, Inc. (NASDAQ:IBIO), an AI-driven innovator developing therapies for cardiometabolic, obesity and cardiopulmonary diseases announced today the appointment of Elizabeth Stoner, M.D., M.S. to its Board of Directors.

Dr. Stoner is appointed as an independent member of the Board of Directors and as a member of the Compensation Committee, following the transition of Eef Schimmelpennink from this position, who has stepped down from the Board.

“We are excited to welcome Liz to our Board of Directors at a pivotal moment in iBio’s evolution as clinical-staged company,” said Martin Brenner, Ph.D., DVM, Chief Executive Officer and Chief Scientific Officer. “Liz brings decades of research and development leadership, with experience advancing programs globally and building companies from early stages through value inflection points. These skills, along with her deep understanding of the biotech investment industry, will be highly valuable as we are embarking on our first human clinical trial. I look forward to working closely with Liz as we lead the advancement of developing differentiated therapies for the potential treatment of obesity and pulmonary hypertension associated with heart failure with preserved ejection fraction to meaningfully impact the lives of patients. I’d also like to thank Eef, whose leadership, guidance and personal friendship has been invaluable to the Company, the Board and myself.”

Dr. Elizabeth Stoner is an accomplished biotech executive with more than 35 years of experience leading research and development. She currently serves as an Entrepreneur Partner at MPM BioImpact, a world-leading biotechnology investment firm, where she works closely with portfolio companies to guide clinical strategy and development. Over the course of her career, she has held multiple senior leadership roles, including serving as interim Chief Executive Officer of Semma Therapeutics and as Founder, Chief Medical Officer, and Chief Development Officer of Rhythm Pharmaceuticals.

Earlier in her career, Dr. Stoner was Senior Vice President of Global Clinical Development Operations at Merck Research Laboratories, where she led clinical development activities across more than 40 countries and played a key role in the development of major commercial therapies. Her experience spans endocrine, metabolic, and cardiovascular programs, as well as broad expertise in global regulatory and clinical execution.

Dr. Stoner currently serves on the boards of multiple biotechnology companies, including Antiva Biosciences and LIB Therapeutics and is actively involved in academic and clinical advisory organizations.

“I am pleased to be joining iBio’s Board of Directors at this very exciting time for the Company, on the verge of becoming a clinical-staged biotech company,” commented Dr. Stoner. “I look forward to working with my fellow directors and an incredible management team to progress IBIO-610, IBIO-600, and other assets into the clinic.”

About iBio, Inc.

iBio (Nasdaq: IBIO) is a cutting-edge biotech company leveraging AI and advanced computational biology to develop next-generation biopharmaceuticals for cardiometabolic and cardiopulmonary diseases, obesity, cancer and other hard-to-treat diseases. By combining proprietary 3D modeling with innovative drug discovery platforms, iBio is creating a pipeline of breakthrough antibody treatments to address significant unmet medical needs. iBio’s mission is to transform drug discovery, accelerate development timelines, and unlock new possibilities in precision medicine. For more information, visit www.ibioinc.com or follow iBio on LinkedIn.

FORWARD-LOOKING STATEMENTS

Certain statements in this press release constitute "forward-looking statements" within the meaning of the federal securities laws. Words such as "may," "might," "will," "should," "believe," "expect," "anticipate," "estimate," "continue," "predict," "forecast," "project," "plan," "intend" or similar expressions, or statements regarding intent, belief, or current expectations, are forward-looking statements. These forward-looking statements are based upon current estimates and assumptions and include statements regarding iBio’s evolution as clinical-staged company; Dr. Stoner’s skills, along with her deep understanding of the biotech investment industry, being valuable to the Company as it is embarking on its first human clinical trial; iBio leading the advancement of developing differentiated therapies for the potential treatment of obesity and PH-HFpEF to meaningfully impact the lives of patients; the Company becoming a clinical-staged biotech company; Dr. Stoner working with her fellow directors and an incredible management team to progress IBIO-610, IBIO-600, and the other assets into the clinic; Dr. Stoner’s expected contributions as a Board member; the Company’s ability to leverage AI and advanced computational biology to develop next-generation biopharmaceuticals for cardiometabolic and cardiopulmonary diseases, obesity, cancer and other hard-to-treat diseases; iBio’s ability to combine its proprietary 3D modeling with its innovative drug discovery platforms to create a pipeline of breakthrough antibody treatments to address significant unmet medical needs; and iBio’s ability to transform drug discovery, accelerate development timelines, and unlock new possibilities in precision medicine. While iBio believes these forward-looking statements are reasonable, undue reliance should not be placed on any such forward-looking statements, which are based on information available to us on the date of this release. These forward-looking statements are subject to various risks and uncertainties, many of which are difficult to predict that could cause actual results to differ materially from current expectations and assumptions from those set forth or implied by any forward-looking statements. Important factors that could cause actual results to differ materially from current expectations include, among others, the ability of iBio to commence its planned clinical trials for IBIO-610, IBIO-600, and its other assets; the ability of Dr. Stoner to contribute to the Company as expected; iBio’s ability to obtain regulatory approvals for commercialization of its product candidates, or to comply with ongoing regulatory requirements; regulatory limitations relating to iBio’s ability to promote or commercialize its product candidates for specific indications; acceptance of iBio’s product candidates in the marketplace and the successful development, marketing or sale of products; and whether iBio will incur unforeseen expenses or liabilities or other market factors; and the other factors discussed in iBio’s filings with the SEC including its Annual Report on Form 10-K for the year ended June 30, 2025 and its subsequent filings with the SEC on Forms 10-Q and 8-K. The information in this release is provided only as of the date of this release, and iBio undertakes no obligation to update any forward-looking statements contained in this release on account of new information, future events, or otherwise, except as required by law.

Contact:

iBio, Inc. 
Investor Relations 
ir@ibioinc.com 

Ignacio Guerrero-Ros, Ph.D., or David Schull
Russo Partners, LLC
Ignacio.guerrero-ros@russopartnersllc.com
David.schull@russopartnersllc.com
(858) 717-2310 or (646) 942-5604


FAQ

Who is Elizabeth Stoner and why did iBio (IBIO) appoint her to the board on May 8, 2026?

She is a biotech executive with over 35 years' R&D leadership experience. According to company, her global clinical development and investment‑industry background is intended to guide clinical strategy as iBio advances programs into human trials.

What role will Dr. Stoner hold at iBio (IBIO) and what committee assignment does she have?

Dr. Stoner joins as an independent director and a member of the Compensation Committee. According to company, she will also advise on clinical development as the firm moves IBIO-610 and IBIO-600 toward the clinic.

How does the board change affect iBio's (IBIO) clinical plans and programs?

The appointment adds clinical and regulatory experience to the board ahead of first‑in‑human studies. According to company, Dr. Stoner's background supports program advancement for IBIO-610, IBIO-600 and other assets into clinical testing.

Which director left iBio's board when Elizabeth Stoner joined on May 8, 2026?

Eef Schimmelpennink stepped down from the board and the Compensation Committee role. According to company, the transition coincided with Dr. Stoner's appointment.

Will Elizabeth Stoner's appointment likely change iBio's (IBIO) strategic focus or investor outlook?

Her appointment brings biotech development and investor‑relations expertise to the board. According to company, she is expected to support clinical and corporate strategy as the company becomes clinical‑staged.