InVivo Therapeutics Announces Completion of Enrollment for the INSPIRE 2.0 Acute Spinal Cord Injury Study
InVivo Therapeutics Holdings Corp. (Nasdaq: NVIV) has completed enrollment in its INSPIRE 2.0 Study, a 20-patient randomized trial aimed at enhancing clinical evidence for its Neuro-Spinal Scaffold™. The study consists of 10 subjects in each arm and is focused on patients with acute spinal cord injury. CEO Richard Toselli highlighted this achievement as a significant advancement and expects to report topline data in Q1 2023. Principal Investigator Kee Kim called the completion of enrollment a major milestone for spinal cord injury treatment.
- Completed enrollment in the INSPIRE 2.0 Study, marking significant progress.
- Study designed to enhance existing clinical evidence for Neuro-Spinal Scaffold™.
- The success of the INSPIRE 2.0 Study is contingent on the outcome of the topline data, which may not meet expectations.
Topline data expected to be reported in Q1 2023
“Reaching full enrollment in our INSPIRE 2.0 study is a significant advancement in our research and development efforts towards a potential treatment for spinal cord injury,” said
For more details on the Company’s INSPIRE 2.0 Study, please visit this link.
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Any statements contained in this press release that do not describe historical facts may constitute forward-looking statements within the meaning of the federal securities laws. These statements can be identified by words such as “believe,” “anticipate,” “intend,” “estimate,” “will,” “may,” “should,” “expect” and similar expressions, and include statements regarding the company’s expectation regarding the timing for the announcement of topline data and ability to serve the spinal cord injury patient population. Any forward-looking statements contained herein are based on current expectations and are subject to a number of risks and uncertainties. Factors that could cause actual future results to differ materially from current expectations include, but are not limited to, risks and uncertainties relating to: the company’s ability to obtain additional funding to support the ongoing clinical and potential commercialization program for the investigational Neuro-Spinal Scaffold™, the varied interpretation of clinical data, the timing, cost and expense of regulatory filings, the potential for regulatory authorities granting or delaying approval for our Neuro-Spinal Scaffold, and other risks associated with the company’s business, research, product development, regulatory approval, marketing and distribution plans and strategies identified and described in more detail in the company’s Quarterly Report on Form 10-Q for the quarter ended
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