Spero Therapeutics to Provide Business Update and Report Third Quarter 2020 Financial Results on Thursday, November 5, 2020

Rhea-AI Summary

Spero Therapeutics, Inc. (Nasdaq: SPRO) announced a conference call on November 5, 2020, at 4:30 p.m. EST to discuss its third quarter 2020 financial results and business updates. The company is focused on developing treatments for multi-drug resistant bacterial infections and rare diseases. Spero's lead candidate, tebipenem HBr, showed positive results in its Phase 3 ADAPT-PO trial for complicated urinary tract infections. Additionally, Spero is advancing SPR720 for rare pulmonary diseases and SPR206 for multi-drug resistant infections in hospitals.

Positive

• Positive top-line results from Phase 3 ADAPT-PO trial for tebipenem HBr.
• Advancement of SPR720 for rare pulmonary diseases.
• Development of SPR206 targeting MDR Gram-negative infections.

Negative

• None.

CAMBRIDGE, Mass., Oct. 29, 2020 (GLOBE NEWSWIRE) -- Spero Therapeutics, Inc. (Nasdaq: SPRO), a multi-asset clinical-stage biopharmaceutical company focused on identifying, developing and commercializing treatments in high unmet need areas involving multi-drug resistant bacterial infections and rare diseases, today announced that it will host a conference call and live audio webcast on November 5, 2020 at 4:30 p.m. EST to report its third quarter 2020 financial results and provide an update on its business and pipeline.

To access the call, please dial (800) 239-9838 (domestic) or (323) 794-2551 (international) and refer to conference ID 8427958. The audio webcast can be accessed under “Events and Presentations” in the Investor and Media section of the Company’s website at www.sperotherapeutics.com. The archived webcast will also be available on Spero’s website for 30 days following the call.

About Spero Therapeutics
Spero Therapeutics, Inc. is a multi-asset, clinical-stage biopharmaceutical company focused on identifying, developing and commercializing novel treatments for multidrug-resistant (MDR) bacterial infections and rare diseases.

Spero’s lead product candidate, tebipenem HBr (tebipenem pivoxil hydrobromide; formerly SPR994), is being developed as the first oral carbapenem antibiotic for use in complicated urinary tract infections (cUTI) and acute pyelonephritis (AP). In September 2020, Spero announced positive top-line results from its Phase 3 ADAPT-PO clinical trial of tebipenem HBr in cUTI and AP.

Spero is also advancing SPR720, its novel oral therapy product candidate being developed for the treatment of rare, orphan pulmonary disease caused by non-tuberculous mycobacterial (NTM) infections.

Spero also has an IV-administered next generation polymyxin product candidate, SPR206, developed from its potentiator platform that is being developed to treat MDR Gram-negative infections in the hospital setting.

For more information, visit https://sperotherapeutics.com.

Spero Investor and Media Contact:
Sharon Klahre
Vice President, Investor Relations
857-242-1547
IR@sperotherapeutics.com

FAQ

What date will Spero Therapeutics report its Q3 2020 financial results?

Spero Therapeutics will report its Q3 2020 financial results on November 5, 2020.

What is Spero Therapeutics' lead product candidate?

Spero Therapeutics' lead product candidate is tebipenem HBr, an oral carbapenem antibiotic.

What clinical trial results did Spero announce in September 2020?

In September 2020, Spero announced positive top-line results from its Phase 3 ADAPT-PO clinical trial of tebipenem HBr.

What is the focus of Spero Therapeutics?

Spero Therapeutics focuses on developing treatments for multi-drug resistant bacterial infections and rare diseases.