CERC: Encouraging Proof-of-Concept Data for CERC-002 in COVID-19 ARDS…
NASDAQ:CERC
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Business Update
Encouraging Proof-of-Concept Data for CERC-002 in ARDS
In January 2021, Cerecor, Inc. (NASDAQ:CERC) announced proof-of-concept data from the exploratory Phase 2 clinical trial of CERC-002 in hospitalized patients with COVID-19 ARDS (NCT04412057). A total of 83 patients (82 treated) were randomized 1:1 to receive standard of care plus either a single dose of CERC-002 (16 mg/kg, maximum 1200 mg) or placebo. Since the protocol allowed for the use of high-flow oxygen prior to randomization (which was part of the definition of ‘respiratory failure’, the primary outcome), the intent-to-treat (ITT) population included 62 patients for analysis of the primary endpoint.
CERC-002 is a monoclonal antibody targeted against LIGHT (Lymphotoxin-like, exhibits Inducible expression, and competes with HSV Glycoprotein D for HVEM, a receptor expressed by T lymphocytes [part of the Tumor Necrosis Super Family 14]), an inflammatory cytokine that is involved in stimulating T cells and the innate immune response (Ward-Kavanagh et al., 2016). It is known to induce the expression of other proinflammatory cytokines such as IL-6 and GM-CSF (Antunes et al., 2018). In addition, its expression is induced by rhinovirus infection and it is involved in airway remodeling driven by allergens (Mehta et al., 2018).
The following graph shows the change in free LIGHT levels in patients over the treatment period. The average LIGHT levels were similar between cohorts, with LIGHT levels approximately 100 pg/mL higher in patients ≥60 years of age. The reduction in light levels by CERC-002 is particularly impressive as it was administered in addition to corticosteroids, which approximately 90% of patients received. We anticipate additional data on LIGHT levels out to Day 28 at the next update.
The primary endpoint of the trial was the proportion of patients alive and free of respiratory failure over the 28-day study period, with respiratory failure defined as endotracheal intubation and mechanical ventilation, oxygen delivered by high-flow nasal cannula, noninvasive positive pressure ventilation, or extracorporeal membrane oxygenation. The results showed that a single treatment of CERC-002 increased the proportion of patients alive and free of respiratory failure over the 28-day study period compared to placebo (OR = 2.62; P=0.059), particularly in patients ≥60 years of age (OR = 3.38; P=0.054) as shown in the following figure.
In addition to showing a positive trend for the primary endpoint, there were clear trends evident for CERC-002 to decrease the need for invasive ventilation and reduce the risk of 28-day mortality, as shown in the following figures. Both of these effects were driven by results in patients ≥60 years of age. While the results did not hit statistical significance, likely due to the low number of events, the data will serve as a guide for properly powering a pivotal trial.
Regarding safety, CERC-002 was well tolerated at a single dose of 16 mg/kg (1,200 mg maximum dose) with no drug-related serious adverse events. In addition, there was no evidence of increased infections or other adverse events related to immunosuppression, with the majority of adverse events reported as mild or moderate.
Looking ahead, we anticipate 60-day follow up data to be reported during the first quarter of 2021, with the full data set presented a scientific conference later this year. In addition, the company will conduct an ‘End-of-Phase 2’ meeting with the FDA to discuss the design of a registration trial as well as filing for Breakthrough Therapy Designation.
Financial Update
Cerecor recently completed a public offering that included the exercise by the underwriters of their option to purchase an additional approximately 1.6 million shares, which increased the total offered through the public offering to approximately 14.0 million and approximately 1.7 million prefunded warrants. This resulted in gross proceeds to the company of approximately $40.7 million. Following the offering, we estimate that the company has approximately $60 million in cash and cash equivalents and approximately 89 million shares outstanding, with a fully diluted share count of approximately 111 million.
Conclusion
We are excited about the data for CERC-002 in COVID-19 ARDS patients, particularly since the drug appears to exert the greatest effect in patients ≥60 years of age, a cohort that is desperately in need of more effective therapies. In addition to providing proof-of-concept data as a COVID-19 treatment, we believe the data presented by Cerecor also serves as excellent proof-of-concept as a potential treatment for non-COVID-19 ARDS patients, which is also a critical situation as there are no pharmacological treatments specifically for ARDS and approximately 40% of hospitalized patients die from it. Outside of ARDS, we anticipate initial data from a trial of CERC-002 in severe pediatric onset Crohn’s disease in the first quarter of 2021. Based on the CERC-002 results and its potential in ARDS we have increased our valuation to $9 per share.
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