GlobeNewswire Inc | Mar 8, 2021 04:01PM EST

March 08, 2021

? Announced CERC-002 significantly reduced respiratory failure and mortality in Phase 2 clinical trial in patients hospitalized with COVID-19 ARDS ? Improved financial position with $18.9M of cash on hand as of December 31, 2020 and $37.6M of net proceeds raised in January 2021 ? Poised to deliver significant number of clinical and regulatory catalysts in 2021

ROCKVILLE, Md. and CHESTERBROOK, Pa., March 08, 2021 (GLOBE NEWSWIRE) -- Cerecor Inc. (NASDAQ: CERC), a biopharmaceutical company focused on becoming a leader in development and commercialization of treatments for rare and orphan diseases, today announced recent business progress and year-end financial results for 2020.

Looking back, 2020 was a very productive and transformative year for Cerecor highlighted by swift transition post the merger with Aevi Genomic Medicine, improving the financial position of the company and initiating clinical trials across our pipeline, said Mike Cola, Chief Executive Officer of Cerecor. 2021 started strong with positive Phase 2 data from CERC-002, our novel anti-LIGHT drug candidate in development for the treatment of COVID-19 ARDS. We have recently filed both Breakthrough Therapy and Fast Track Designations and anticipate meeting with the FDA to discuss next steps in this program soon. Overall, we believe 2021 will be a breakout year for Cerecor and look forward to building on early momentum with important pipeline updates across our immunology, oncology, and rare disease assets.

Business Updates:

Cerecor announced CERC-002 significantly reduced respiratory failure and ? mortality in Phase 2 clinical trial in Patients hospitalized with COVID-19 ARDS. ? The Company closed an underwritten public offering for net proceeds of approximately $37.6 million in January. Dr. Gilla Kaplan was appointed to the Board of Directors in October of 2020 ? bringing decades of experience in rare diseases and immune-inflammatory disorders. Schond Greenway was appointed as Chief Financial Officer, with an ? established focus on investor relations to further help capitalize the company.

Program Updates:

? CERC-002: Anti-LIGHT monoclonal antibody in clinical development for COVID-19 ARDS and severe pediatric onset Crohn?s disease. Completed double-blinded, placebo-controlled Phase 2 proof-of-concept study of CERC-002 in cytokine storm-induced COVID-19 ARDS. Final analysis inclusive of the 60-day safety update in the randomized placebo-controlled study demonstrated CERC-002 was statistically significant in reducing respiratory failure and mortality at Day 28 in patients hospitalized with COVID-19-associated pneumonia and mild to moderate acute respiratory distress syndrome (ARDS), the primary endpoint, (n=62, p=0.044) At both the 28-day and the 60-day final timepoints, an approximately 50% trend in mortality reduction (22.5% vs 10.8%) was observed. CERC-002 appeared safe and well-tolerated on top of standard of care including high dose steroids (>90%) and remdesivir (>65%). Cerecor has submitted applications to the FDA for Breakthrough Therapy and Fast Track Designations and plans to meet with FDA to discuss the path to Emergency Use Authorization (EUA) and full approval. The company is continuing to enroll patients in its Phase 1b trial in severe pediatric-onset Crohn?s disease with initial data expected in the second quarter and is exploring the applicability of CERC-002 in non-COVID-19 ARDS. ? CERC-007: Anti-IL-18 monoclonal antibody for the treatment of multiple myeloma (MM) and Still's disease (AOSD and sJIA). In December 2020, announced FDA Acceptance of two Investigational New Drug Applications for CERC-007 for the treatment of Still?s disease and for the treatment of relapsed or refractory multiple myeloma (MM). Following the first patient dosed in the Phase 1b clinical trial in patients with relapsed or refractory MM in December, the Company has successfully completed enrollment of the first patient cohort and looks to begin dosing cohort two. Initial data anticipated from Phase 1b clinical trial in adult onset Still?s disease in the second quarter of 2021. ? CERC-006: Dual mTORC1 and mTORC2 small molecule inhibitor for complex lymphatic malformations. Initial data anticipated from proof-of-concept study in the second quarter of 2021. ? CERC-800 programs (CERC-801, CERC-802, and CERC-803): Therapeutic doses of monosaccharide therapies for congenital disorders of glycosylation (CDGs). CERC-801 ? In collaboration with the Frontiers in Congenital Disorders of Glycosylation Consortium clinical program, data are anticipated from the pivotal trial evaluating the safety and efficacy of D-galactose in patients suffering from Phosphoglucomutase-1 deficiency related congenital disorders of glycosylation (PGM1-CDG) in second half of 2021. CERC-802 ? Data anticipated from the pivotal trial evaluating the safety and efficacy of D-mannose in patients suffering from Mannose phosphate isomerase deficiency related CDG (MPI-CDG) in second half of 2021. CERC-803 ? Clearance to proceed on the Investigational New Drug Application and received Fast Track Designation from the FDA in the fourth quarter 2020. Data anticipated from the pivotal trial evaluating the safety and efficacy of L-fucose in patients suffering from Leukocyte Adhesion Deficiency II (LAD II) in second half of 2021.

2020 Financial Update:

As of December 31, 2020, Cerecor had $18.9 million in cash and cash equivalents which is a significant increase over the prior year balance of $3.6 million. Furthermore, in January 2021, the Company closed an underwritten public offering for net proceeds of approximately $37.6 million.

There were significant increases to most operating expenses, net loss and net loss per share related to the merger with Aevi Genomic Medicine that occurred in February 2020 (the Aevi Merger). Notably, research and development expense for the year ended December 31, 2020 significantly increased to $32.2 million, which was driven by activities to advance the Companys expanded pipeline as a result of the Aevi Merger. There was a $25.5 million acquired in-process research and development (IPR&D) charge in 2020 directly related to the Aevi Merger. General and administrative expense increased to $17.4 million; the largest driver of such increase was stock-based compensation and other expenses related to leadership changes as a result of the Aevi Merger.

We believe these significant investments in our expanded pipeline and leadership team will lead to value driving milestones as our pipeline progresses toward commercialization.

Condensed Consolidated Balance Sheets

December 31, 2020 2019 Assets (in thousands)Current assets: Cash and cash equivalents $ 18,919 $ 3,609 Accounts receivable, net 2,177 1,002 Other receivables 2,208 4,241 Inventory, net 3 21 Prepaid expenses and other current assets 2,660 707 Restricted cash, current portion 38 17 Investment in Aytu - 7,629 Current assets of discontinued operations - 498 Total current assets 26,005 17,724 Property and equipment, net 1,607 1,448 Intangible assets, net 1,585 2,426 Goodwill 14,409 14,409 Restricted cash, net of current portion 149 102 Total assets $ 43,755 $ 36,109 Liabilities and stockholders? equity Current liabilities: Accounts payable $ 2,574 $ 2,078 Accrued expenses and other current liabilities 11,310 5,640 Income taxes payable - 552 Current liabilities of discontinued operations 1,341 3,891 Total current liabilities 15,225 12,161 Royalty obligation 2,000 - Deferred tax liability, net 90 86 Other long-term liabilities 1,878 1,112 Long-term liabilities of discontinued operations - 1,755 Total liabilities 19,193 15,114 Stockholders? equity: Common stock?$0.001 par value; 200,000,000 sharesauthorized at December31, 2020 and 2019;75,004,127 and 44,384,222 shares issued and 75 44 outstanding at December31, 2020 and 2019,respectivelyPreferred stock?$0.001 par value; 5,000,000 sharesauthorized at December 31, 2020 and 2019; 1,257,143 1 3 and 2,857,143 shares issued and outstanding atDecember31, 2020 and 2019, respectivelyAdditional paid-in capital 202,276 135,239 Accumulated deficit (177,790 ) (114,291 )Total stockholders? equity 24,562 20,995 Total liabilities and stockholders? equity $ 43,755 $ 36,109 The condensed consolidated balance sheets at December 31, 2020 and 2019 havebeen derived from the financial statements but do not include all of theinformation and footnotes required by accounting principles generally acceptedin the United States for complete financial statements

Condensed Consolidated Statements of Operations

Year Ended December 31, 2020 2019 (in thousands, except per share data)Revenues: Product revenue, net $ 6,699 $ 6,650 License and other revenue - 100 Total revenues, net 6,699 6,750 Operating expenses: Cost of product sales 300 (567 )Research and development 32,193 11,764 Acquired in-process research and development 25,549 - General and administrative 17,418 10,124 Sales and marketing 2,341 1,484 Amortization expense 1,741 1,339 Change in fair value of contingent consideration - (1,256 )Total operating expenses 79,542 22,888 (72,843 ) (16,138 )Other income: Change in fair value of Investment in Aytu 5,208 54 Other income (expense), net 409 (28 )Interest income, net 49 121 Total other income, net from continuing 5,666 147 operationsLoss from continuing operations before taxes (67,177 ) (15,991 )Income tax (benefit) expense (2,793 ) 280 Loss from continuing operations $ (64,384 ) $ (16,271 )Income from discontinued operations, net of tax 884 198 Net loss $ (63,500 ) $ (16,073 ) Net (loss) income per share of common stock, basic and diluted:Continuing operations $ (0.87 ) $ (0.28 )Discontinued operations 0.01 0.00 Net loss per share of common stock, basic and $ (0.86 ) $ (0.28 )diluted Net (loss) income per share of preferred stock, basic and diluted:Continuing operations $ (4.38 ) $ (1.42 )Discontinued operations 0.06 0.01 Net loss per share of preferred stock, basic and $ (4.32 ) $ (1.41 )diluted The condensed consolidated statements of operations for the years endedDecember 31, 2020 and 2019 have been derived from the financial statements butdo not include all of the information and footnotes required by accountingprinciples generally accepted in the United States for complete financialstatements.

About Cerecor

Cerecor is a biopharmaceutical company focused on becoming a leader in the development and commercialization of treatments for rare and orphan diseases. The company is advancing its clinical-stage pipeline of innovative therapies that address unmet patient needs within rare and orphan diseases. The company's rare disease pipeline includes CERC-801, CERC-802 and CERC-803, which are in development for congenital disorders of glycosylation and CERC-006, an oral mTORc1/c2 inhibitor in development for the treatment of complex lymphatic malformations. The company is also developing two monoclonal antibodies, CERC-002, and CERC-007. CERC-002 targets the cytokine LIGHT (TNFSF14) and is in clinical development for treatment of severe pediatric-onset Crohn's disease, and COVID-19 acute respiratory distress syndrome. CERC-007 targets the cytokine IL-18 and is in clinical development for the treatment of Stills disease (adult onset Stills disease (AOSD) and systemic juvenile idiopathic arthritis (sJIA)), and multiple myeloma (MM). CERC-006, 801, 802 and 803 have all received Orphan Drug Designation and Rare Pediatric Disease Designation, which makes all four eligible for a priority review voucher upon FDA approval.

For more information about Cerecor, please visit www.cerecor.com.

Forward-Looking Statements

This press release may include forward-looking statements made pursuant to the Private Securities Litigation Reform Act of 1995. Forward-looking statements are statements that are not historical facts. Such forward-looking statements are subject to significant risks and uncertainties that are subject to change based on various factors (many of which are beyond Cerecors control), which could cause actual results to differ from the forward-looking statements. Such statements may include, without limitation, statements with respect to Cerecors plans, objectives, projections, expectations and intentions and other statements identified by words such as projects, may, might, will, could, would, should, continue, seeks, aims, predicts, believes, expects, anticipates, estimates, intends, plans, potential, or similar expressions (including their use in the negative), or by discussions of future matters such as: the development of product candidates or products; timing and success of trial results and regulatory review; potential attributes and benefits of product candidates; and other statements that are not historical. These statements are based upon the current beliefs and expectations of Cerecors management but are subject to significant risks and uncertainties, including: drug development costs, timing and other risks, including reliance on investigators and enrollment of patients in clinical trials, which might be slowed by the COVID-19 pandemic; regulatory risks; Cerecor's cash position and the potential need for it to raise additional capital; general economic and market risks and uncertainties, including those caused by the COVID-19 pandemic; and those other risks detailed in Cerecors filings with the Securities and Exchange Commission. Actual results may differ from those set forth in the forward-looking statements. Except as required by applicable law, Cerecor expressly disclaims any obligations or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in Cerecors expectations with respect thereto or any change in events, conditions, or circumstances on which any statement is based.

For media and investor inquiries

Chris BrinzeyWestwicke, an ICR Companychris.brinzey@westwicke.com339-970-2843

or

Schond L. GreenwayInvestor RelationsChief Financial OfficerCerecor Inc.sgreenway@cerecor.com610-522-6200 office