Iveric Bio Announces Agreement for Up to $250 Million in Non-Dilutive Debt Financing with Hercules Capital and Silicon Valley Bank
IVERIC bio, Inc. (Nasdaq: ISEE) has secured a $250 million term loan debt financing facility from Hercules Capital (NYSE: HTGC) and Silicon Valley Bank. This non-dilutive financing strengthens the company's balance sheet, allowing it to fund the potential launch of Zimura® (avacincaptad pegol) in the U.S., pending regulatory approval. The initial $50 million will be drawn in July 2022, with additional funds contingent on achieving performance milestones. Iveric plans to report data from the GATHER2 clinical trial in September 2022, crucial for Zimura's development.
- Secured $250 million in non-dilutive debt financing, enhancing balance sheet strength.
- The financing supports potential commercial launch of Zimura, focusing on geographic atrophy.
- Initial $50 million expected to be available immediately, promoting cash flow stability.
- Additional $150 million contingent on performance milestones, introducing execution risk.
- Dependence on future regulatory approval and clinical trial outcomes for financial prospects.
“We are grateful to secure this non-dilutive financing as it further strengthens our balance sheet and provides financial flexibility as we look to fund the potential commercial launch of Zimura® (avacincaptad pegol) in geographic atrophy (GA) in
“Hercules is excited to collaborate with
“Iveric Bio is doing important work to advance potential treatments for GA and other retinal diseases,” said
Under the terms of the facility the Company is borrowing
Additional details of the credit facility agreement are filed with the
About
Iveric Bio Forward-looking Statements
Any statements in this press release about Iveric Bio’s future expectations, plans and prospects constitute forward-looking statements for purposes of the safe harbor provisions under the Private Securities Litigation Reform Act of 1995. Forward-looking statements include any statements about the Company’s strategy, future operations and future expectations and plans and prospects for the Company, and any other statements containing the words “anticipate,” “believe,” “estimate,” “expect,” “intend”, “goal,” “may”, “might,” “plan,” “predict,” “project,” “seek,” “target,” “potential,” “will,” “would,” “could,” “should,” “continue,” and similar expressions. In this press release, the Company’s forward looking statements include statements about its expectations regarding its development and regulatory strategy for Zimura, including the timing of receipt of topline data from the GATHER2 clinical trial, its ability to use its completed GATHER1 trial as a Phase 3 trial for purposes of seeking regulatory approval, the potential commercial launch of Zimura, and the potential utility of Zimura for treating geographic atrophy (GA), if approved. Such forward-looking statements involve substantial risks and uncertainties that could cause the Company’s development programs, future results, performance, or achievements to differ significantly from those expressed or implied by the forward-looking statements. Such risks and uncertainties include, among others, those related to the progress and success of research and development programs and clinical trials, developments from the scientific and medical community, expectations for regulatory matters, reliance on clinical trial sites, contract development and manufacturing organizations and other third parties, establishment of manufacturing capabilities, need for additional financing, negotiation and consummation of business development transactions and other factors discussed in the “Risk Factors” section contained in the quarterly and annual reports that the Company files with the Securities and
ISEE-G
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Investor Contact:
Senior Vice President, Investor Relations
kathy.galante@ivericbio.com
or
Media Contact:
Senior Director,
jeannie.neufeld@ivericbio.com
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