InflaRx Achieves Significant Milestone with GOHIBIC Approval

InflaRx Receives Approval for GOHIBIC in Europe

InflaRx N.V. (NASDAQ: IFRX) recently celebrated the remarkable achievement of receiving marketing authorization from the European Commission for GOHIBIC (vilobelimab). This groundbreaking drug is designated for adult patients suffering from SARS-CoV-2-induced acute respiratory distress syndrome (ARDS). The approval underscores the urgency for effective treatments in critical care settings, particularly for patients already undergoing systemic corticosteroid therapy and invasive mechanical ventilation.

Significant Impact on Critical Care

The approval of GOHIBIC is a historic step, being the first of its kind authorized within the European Union. The Chief Executive Officer and Founder of InflaRx, Prof. Niels C. Riedemann, expressed pride in this milestone, emphasizing the company's commitment to addressing the needs of ICU patients. He acknowledged the critical support received from healthcare professionals and families participating in pivotal clinical studies that helped pave the way for this marketing authorization.

Partnership and Distribution Plans

The authorization is not only valid across all 27 EU member states but also extends to Iceland, Liechtenstein, and Norway. InflaRx is exploring various commercial partnering and distribution strategies within the EU while keeping a close eye on its operational costs, ensuring that such strategies do not negatively impact its financial stability.

Understanding GOHIBIC (vilobelimab)

GOHIBIC (vilobelimab) has been granted marketing authorization under special circumstances due to the rarity of ARDS conditions among patients with COVID-19. This decision reflects the positive benefit/risk assessment associated with vilobelimab. The key trial supporting its approval is the multicenter Phase 3 PANAMO study, recognized as one of the largest randomized, double-blind trials focusing on mechanically ventilated COVID-19 patients. Results demonstrated a substantial 23.9% reduction in 28-day all-cause mortality compared to those receiving placebo, reinforcing the potential for vilobelimab to enhance survival rates.

Future Developments in the U.S.

In addition to its European successes, vilobelimab has been granted Emergency Use Authorization in the U.S. by the FDA, specifically for hospitalized adults with COVID-19 when initiated within 48 hours of receiving invasive mechanical ventilation or ECMO. However, it is important to note that GOHIBIC remains an investigational drug in the U.S., with limited information on safety and efficacy for this indication.

Safety Information and Precautions

Despite its promising therapeutic potential, healthcare professionals must exercise caution, as there are limited clinical data available for vilobelimab. Serious adverse events, such as infections and hypersensitivity reactions, may occur. Monitoring for signs of new infections during treatment is crucial, and any severe allergic reactions necessitate immediate discontinuation of the drug.

The Mechanism Behind Vilobelimab

Vilobelimab operates by targeting the complement system, specifically the C5a factor, which is a vital inflammatory mediator implicated in numerous inflammatory diseases. By inhibiting C5a’s activity, vilobelimab mitigates excessive tissue damage caused by uncontrolled inflammatory responses, presenting a novel approach to treating severe inflammatory conditions.

About InflaRx

Founded in 2007, InflaRx (NASDAQ: IFRX) has established itself as a leader in anti-inflammatory therapeutics. With a focus on leveraging its proprietary anti-C5a technologies, the company aims to develop targeted therapies for various inflammatory diseases. Its commitment to innovation signifies a promising future, with GOHIBIC being just one of its potential game-changers.

Frequently Asked Questions

What is GOHIBIC used for?

GOHIBIC is used for treating adult patients with SARS-CoV-2-induced acute respiratory distress syndrome, especially those receiving mechanical ventilation.

Is GOHIBIC approved in the U.S.?

GOHIBIC has received Emergency Use Authorization in the U.S. for treating hospitalized adults with COVID-19 under specific conditions.

What outcomes were observed in the PANAMO trial?

The PANAMO trial demonstrated a 23.9% reduction in 28-day all-cause mortality for patients treated with vilobelimab compared to placebo.

Are there side effects associated with GOHIBIC?

Common side effects include infections and hypersensitivity reactions, requiring careful monitoring by healthcare providers.

Who is InflaRx?

InflaRx is a biopharmaceutical company focused on developing innovative anti-inflammatory therapeutics, including GOHIBIC for treating severe medical conditions.

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