CAMBRIDGE, Mass., April 16, 2018 (GLOBE NEWSWIRE) -- Spero Therapeutics, Inc. (Nasdaq:SPRO), a multi-asset clinical-stage
biopharmaceutical company focused on identifying, developing and commercializing novel treatments for multidrug-resistant bacterial
infections, announced today one oral presentation and seven poster presentations on SPR741 at the 28th European Congress of
Clinical Microbiology and Infectious Diseases (ECCMID) being held April 21-24, 2018 in Madrid, Spain. Presentations will include
data from the Company’s Phase 1 single-ascending dose (SAD) and multiple-ascending dose (MAD) clinical trial of SPR741 as well as
other preclinical studies of SPR741 as a single agent and in combination with other standard-of-care agents for Gram-negative
infections.
“The data to be presented at ECCMID highlight the anticipated utility of our Potentiator Platform and we believe
validate this novel approach to treat multidrug-resistant Gram-negative infections,” said Ankit Mahadevia, M.D., CEO of Spero
Therapeutics. “We look forward to an eventful 2018 for the Potentiator Program with multiple anticipated catalysts, including Phase
1b drug-drug interaction data for SPR741, and IND-enabling data for SPR206, our second pipeline candidate from the Potentiator
Platform that is designed to be active as a single agent.”
SPR741 is a novel investigational agent that is designed to expand the spectrum and increase the potency of a
partner antibiotic when administered in combination. The Phase I trial of SPR741 being presented at ECCMID demonstrated the drug to
be generally well tolerated in single doses of up to and including 800 mg and at doses up to and including 600 mg every 8 hours for
14 days. A Phase 1b drug-drug interaction trial of SPR741 is ongoing to assess the impact, if any, on the pharmacokinetics of
SPR741 or the pharmacokinetics of the beta-lactam combination drug when the two are dosed together. We continue to expect to
receive top-line data from the SPR741 Phase 1b drug-drug interaction trial during the second quarter of 2018.
The following posters further detail the data from the Phase 1 SPR741 trial:
- Safety of SPR741, a novel polymyxin potentiator, in healthy adults receiving single- and multiple-dose intravenous
administrations
Poster Presentation – P2206; Presenter: Paul Eckburg
Tuesday, April 24, 2018, 12:30 p.m. – 1:30 p.m. CET
- Determination of the pharmacokinetics of single (SAD) and multiple ascending doses (MAD) of SPR741 in healthy volunteers
Poster Presentation – P2233; Presenter: Luke Utley
Tuesday, April 24, 2018, 12:30 p.m. – 1:30 p.m. CET
The SPR741 Phase 1 SAD/MAD clinical trial was a two-part, randomized, double-blind, placebo-controlled,
dose-escalation study designed to evaluate the safety, tolerability, and pharmacokinetics of single and multiple ascending
intravenous doses of SPR741. The study enrolled 96 healthy adult volunteers in cohorts up to and including an 800 mg single dose
and up to and including a 600 mg dose every 8 hours for 14 days. SPR741 was generally well tolerated in single doses of up to and
including 800 mg and at doses up to and including 600 mg every 8 hours for 14 days. SPR741, administered up to 400 mg every 8 hours
for up to 14 days, displayed linear and proportional pharmacokinetics and showed no evidence of accumulation or time dependent
changes in plasma exposure as measured by AUC, Cmax or Ctrough. Renal clearance decreased slightly with dose after 14
days of repeat dosing.
The following posters characterize the activity and synergistic effects of SPR741 in combination with a partner
antibiotic:
- Bactericidal activity of ceftazidime in combination with SPR741 against susceptible, extended-spectrum beta-lactamase
producing, and multi-drug resistant Escherichia coli, Klebsiella pneumoniae, and Enterobacter species
Poster Presentation – P1674; Presenter: Nicole Cotroneo
Monday, April 23, 1:30 p.m. – 2:30 p.m. CET
- Bactericidal activity of piperacillin-tazobactam in combination with SPR741 against susceptible, extended-spectrum
beta-lactamase producing, and multi-drug resistant Escherichia coli, Klebsiella pneumoniae, and Enterobacter
species
Poster Presentation – P1675; Presenter: Nicole Cotroneo
Monday, April 23, 2018, 1:30 p.m. – 2:30 p.m. CET
The in vitro data suggest that the addition of 8 mg/L of SPR741 to ceftazidime or
piperacillin-tazobactam may significantly enhance the antimicrobial potency and cidality of the agents against clinical isolates of
Enterobacteriaceae.
- Antimicrobial activity of Ceftazidime and Piperacillin-Tazobactam tested in combination with a potentiator molecule (SPR741)
against Enterobacteriaceae causing urinary-tract infections
Poster Presentation – P1671; Presenter: Rodrigo E. Mendes
Monday, April 23, 2018, 1:30 p.m. – 2:30 p.m. CET
An assessment of the in vitro activity of ceftazidime or piperacillin-tazobactam in combination with
SPR741 against Gram-negative urinary tract infection, or UTI, pathogens, including Escherichia coli, Klebsiella
pneumoniae, and Enterobacter cloacae, suggests that SPR741 has the ability to extend the potency of these
standard-of-care agents.
- Evaluation of synergistic effects of a potentiator molecule (SPR741) when tested in combination with a series of beta-lactam
agents against a challenge set of Gram-negative pathogens
Poster Presentation – P1672; Presenter: Rodrigo E. Mendes
Monday, April 23, 2018, 1:30 p.m. – 2:30 p.m. CET
The in vitro data suggest that SPR741 significantly potentiates the antimicrobial activity of
ceftazidime, piperacillin-tazobactam, mecillinam and temocillin against a challenge set of pathogens that express a diverse array
of beta-lactam antimicrobial resistance mechanisms, including plasmid AmpC (pAmpC), extended-spectrum β-lactamase (ESBL),
Klebsiella pneumoniae carbapenemase (KPC), metallo-β-lactamase (MBL), and OXA-48-like enzymes.
- In vitro activity of ceftazidime alone and in combination with SPR741 against anaerobic bacteria
Poster Presentation – P1673; Presenter: Aileen Rubio
Monday, April 23, 2018, 1:30 p.m. – 2:30 p.m. CET
An assessment of the MIC90 values suggest that SPR741 or ceftazidime alone, or in combination is
unlikely to significant impact the viability of common anaerobic bacteria, and thus, unlikely to cause significant perturbations to
the gut microbiota.
The following poster characterizes the mechanism of action of SPR741:
- Characterization of SPR741, a potentiating polymyxin B analog, using atomic force microscopy and chemical-genomics profiling
Oral Presentation – O0249; Presenter: Aileen Rubio
Saturday, April 21, 2018, 5:06 p.m. – 5:16 p.m. CET
The outer membrane of Gram-negative bacteria acts as a formidable permeability barrier for some
antibiotics. Studies to assess the impact on the outer membrane and potential mechanism of action of SPR741 suggest that it
acts as an outer membrane disruptor and its potential molecular target may be distinct from the structurally similar compound
polymyxin B nonapeptide.
Complete abstracts for the presentations listed above can be accessed through the ECCMID website.
About the Spero Potentiator Platform
Our Potentiator Platform molecules are designed to treat Gram-negative bacterial infections through the molecules’ interactions
with the bacteria’s outer cell membrane as a monotherapy or by co-administering our Potentiator Platform molecules with existing
antibiotics, thereby making the existing antibiotics more effective by clearing a path for them to enter and kill the bacteria. We
have two Potentiator Platform product candidates – SPR741, our combination IV-administered agent that has demonstrated in
vitro the ability to expand the spectrum and increase the potency of a co-administered antibiotic; and SPR206, our direct
acting IV-administered agent that has demonstrated in vitro activity alone. Both have demonstrated potency
against Gram-negative bacteria, including organisms identified by the Centers for Disease Control and Prevention, or
the CDC, and the World Health Organization, or the WHO, as urgent and serious threats to human health. SPR741 has
demonstrated an ability to potentiate over two dozen existing antibiotics by expanding their activity against Gram-negative
pathogens. SPR206 is designed to also have antibiotic activity as a single agent against MDR and extremely drug resistant, or XDR,
bacterial strains, including variants isolated in Pseudomonas aeruginosa, Acinetobacter baumannii and
carbapenem-resistant Enterobacteriaceae.
The work on these compounds was partially supported by non-dilutive funding from the Office of the Assistant Secretary of
Defense for Health Affairs, through the Peer Reviewed Medical Research Program under Award No. W81XWH-16-2-0019. This work is
also partially supported by the Cooperative Agreement Number IDSEP160030 from ASPR/BARDA and by an award from the Wellcome Trust,
as administrated by CARB-X. The contents of the press release are solely the responsibility of the authors and do not necessarily
represent the official views of CARB-X, the HHS Office of the Assistant Secretary for Preparedness and Response, the National
Institutes of Health or the Wellcome Trust.
About Spero
Spero Therapeutics is a multi-asset, clinical-stage biopharmaceutical company focused on identifying,
developing and commercializing novel treatments for multidrug-resistant (MDR) bacterial infections.
Spero is advancing SPR994, a carbapenem-class antibiotic, which is designed to be the first broad-spectrum oral antibiotic for
use in adults to treat MDR Gram-negative infections.
Spero is also advancing its Potentiator Platform, which it believes will enable the development of drugs that
will expand the spectrum and potency of existing antibiotics, including formerly inactive antibiotics, against Gram-negative
bacteria. The product candidates are two IV-administered agents, SPR741 and SPR206, designed to treat MDR Gram-negative infections
in the hospital setting.
Spero is also advancing SPR720, its novel oral therapy product candidate designed for the treatment of pulmonary
non-tuberculous mycobacterial (NTM) infection, an orphan infectious disease.
For more information, visit https://sperotherapeutics.com.
Forward Looking Statements
This press release may contain forward-looking statements. These statements include, but are not limited
to, statements about the initiation, timing, progress and results of the Company’s preclinical studies and clinical trials and the
Company’s research and development programs, including statements regarding management’s assessment of the results of such
preclinical studies and clinical trials, the timing of clinical data, the Company’s cash forecast and anticipated expenses and the
sufficiency of the Company’s cash resources. In some cases, forward-looking statements can be identified by terms such as
“may,” “will,” “should,” “expect,” “plan,” “aim,” “anticipate,” “could,” “intent,” “target,” “project,” “contemplate,” “believe,”
“estimate,” “predict,” “potential” or “continue” or the negative of these terms or other similar expressions. Actual results
may differ materially from those indicated by such forward-looking statements as a result of various important factors, including
whether results obtained in preclinical studies and clinical trials will be indicative of results obtained in future clinical
trials; whether the Company’s product candidates will advance through the preclinical development and clinical trial process on a
timely basis, or at all; whether the results of such trials will warrant submission for approval from the United States Food
and Drug Administration or equivalent foreign regulatory agencies; whether the Company’s cash resources will be sufficient to
fund its continuing operations for the periods and/or trials anticipated; and other factors discussed in the “Risk Factors” section
of the Company’s Annual Report on Form 10-K filed with the Securities and Exchange Commission on April 2, 2018, and
risks described in other filings the Company may make with the Securities and Exchange Commission in the future.
The forward-looking statements included in this press release represent the Company’s views as of the date of this press
release. The Company anticipates that subsequent events and developments will cause its views to change. However, while
the Company may elect to update these forward-looking statements at some point in the future, it specifically disclaims any
obligation to do so. These forward-looking statements should not be relied upon as representing the Company’s views as of any
date subsequent to the date of this press release.
Spero Investor Contact:
Sharon Klahre
Director, Investor Relations
857-242-1547
IR@sperotherapeutics.com