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Government Contracts
6 Months Ended
Jun. 30, 2019
Contractors [Abstract]  
Government Contracts

10.

Government Contracts

 

BARDA

 

In July 2018, the Company was awarded a contract from Biomedical Advanced Research and Development Authority (“BARDA”) of up to $44.2 million to develop SPR994 for the treatment of complicated urinary tract infections (“cUTI”) caused by antibiotic resistant Gram-negative bacteria and for assessment against biodefense pathogens. The award committed initial funding of $15.7 million over a three-year base period from July 1, 2018 to June 30, 2021 for cUTI development activities. In May 2019, the contract was modified to include additional funding of $2.5 million for SPR994, increasing the amount of initial committed funding from $15.7 million to $18.1 million and increasing the overall potential award to $46.7 million. The balance of the award is subject to BARDA exercising two options. The exercise of the first option would entail funding of $13.6 million and is exercisable by BARDA subject to the Company achieving specified milestones related to, among other things, clinical progress and data. The exercise of the second option would entail funding of $14.9 million and is exercisable by BARDA subject, among other things, satisfactory progress and results from the biodefense studies described below. The Company recognized $1.5 million and $5.1 million of revenue under this award during the three and six months ended June 30, 2019, respectively.

 

As part of an inter-agency collaboration between BARDA and the Defense Threat Reduction Agency (“DTRA”), a series of studies to assess the efficacy of SPR994 in the treatment of infections caused by biodefense threats such as anthrax, plague and melioidosis will be conducted by the U.S. Army Medical Research Institute of Infectious Diseases (“USAMRIID”) under the direction of Spero. Because the FDA requires data from a human pneumonic disease as supportive of use of an antibiotic to treat a biothreat infection, the scope of the BARDA award includes the assessment of SPR994 levels in the lung of healthy volunteers as well as a proof of concept clinical trial in pneumonia patients, an indication for which tebipenem, SPR994's active pharmaceutical ingredient, is currently approved in Japan for pediatric use.

 

U.S. Department of Defense

 

In September 2016, the Company was awarded a cooperative agreement with the DoD to further develop anti-infective agents to combat Gram-negative bacteria. The agreement was initially structured as a single, two-year $1.5 million award. The performance period has since then been extended through September 29, 2019. The Company is eligible for the full funding from the DoD, and there are no options to be exercised at a later date. The DoD funding supports next-generation potentiator discovery and screening of SPR741 partners. The Company recognizes revenue under this agreement as qualifying expenses are incurred. The Company recognized less than $0.1 million and $0.1 million of revenue under this agreement during the three months ended June 30, 2019 and 2018, respectively. The Company recognized less than $0.1 million and $0.2 million during the six months ended June 30, 2019 and 2018, respectively.

 

NIAID

 

In February 2017, the Company was awarded a grant from NIAID under its Small Business Innovation Research program, to conduct additional preclinical studies of SPR720, the Company’s novel oral bacterial gyrase inhibitor, for the treatment of non-tuberculous mycobacterial infections. The award is structured as a 12-month $0.6 million base period and a $0.4 million option period. Through December 31, 2017, only the base period funds had been committed. In February 2018, NIAID exercised the $0.4 million 12-month option period. In January 2019, the period of performance for this award was extended for an additional 12-month period. The Company recognized less than $0.1 million and $0.1 million of revenue under this agreement during the three months ended June 30, 2019 and 2018, respectively. The Company recognized less than $0.1 million and $0.2 million of revenue under this agreement during the six months ended June 30, 2019 and 2018, respectively.

 

In June 2016, the Company entered into agreements with Pro Bono Bio PLC (“PBB”), a corporation organized under the laws of England, and certain of its affiliates, including PBB Distributions Limited and Ascension Healthcare Development Limited (formerly Cantab Anti-Infectives Limited) (“CAI”), in order to acquire certain intellectual property and government funding arrangements relating to SPR206 (see Note 11). Under these agreements, CAI agreed to submit a request to NIAID to assign the CAI-held NIAID contract to Spero, which was finalized in December 2017. The NIAID contract provides for total development funding of up to $6.3 million, including a base period and three option periods. To date, funding for the base period and the first two option periods totaling $5.7 million have been committed. The Company recognized $0.5 million and $0.3 million of revenue under this agreement during the three months ended June 30, 2019 and 2018, respectively, and $0.8 million and $0.7 million of revenue during the six months ended June 30, 2019 and 2018, respectively under this agreement. Spero shall pay PBB a percentage of funds received from NIAID up to a maximum of $1.3 million, of which $0.3 million was paid upfront to PBB as part of this agreement. The Company recorded less than $0.1 million and $0.1 million in expense associated with amounts payable to PBB under this agreement during the three months ended June 30, 2019 and 2018, respectively, and $0.2 million for both the six months ended June 30, 2019 and 2018, respectively, which have been included within research and development expenses within the condensed consolidated statement of operations and comprehensive loss. 

 

 

CARB-X

 

In April 2017, the Company was awarded a grant from CARB-X, a public-private partnership funded by BARDA within the U.S. Department of Health and Human Services to be used to screen, identify and complete Phase 1 trials with at least one partner compound for SPR741, one of the Company’s Potentiator Platform product candidates. The award committed to funding of $1.5 million over a 12-month period. On March 12, 2018, CARB-X committed an additional $0.4 million related to the first option for a period from December 1, 2017 to March 31, 2018. There will be no additional options exercised under the CARB-X award. As the period of performance under this award ended on March 31, 2018, the Company is no longer recognizing any revenue under this agreement. The Company recognized $0.5 million of revenue under this agreement during the six months ended June 30, 2018.