Kaleido Biosciences Reports First Quarter 2021 Financial Results
Kaleido Biosciences (NASDAQ: KLDO) reported a net loss of $23 million, or $0.58 per share, for Q1 2021, compared to $19.6 million, or $0.64 per share, in Q1 2020. The increased loss was driven by R&D expenses rising to $17.2 million, primarily due to COVID-19 study expenditures. KB109 showed promising results in reducing healthcare utilization and recovery times for mild-to-moderate COVID-19 patients. The company closed a public offering raising approximately $69.4 million and is advancing its IND application for KB109 while expecting topline data for KB295 in ulcerative colitis mid-2021.
- Positive results from KB109 clinical study indicate reduced healthcare utilization and recovery time.
- Successful public offering raised approximately $69.4 million to support continued development.
- Cash and cash equivalents of $92.4 million ensure runway into Q1 2022.
- Net loss of $23.0 million for Q1 2021, an increase from $19.6 million in Q1 2020.
- R&D expenses rose to $17.2 million, indicating higher spending amid clinical trials.
--Positive results in patients with mild-to-moderate COVID-19 demonstrate KB109’s potential to reduce healthcare utilization and recovery time; initiating IND application to support further development--
--Topline data from a clinical study of KB295 in patients with mild-to-moderate ulcerative colitis on track for mid-2021--
LEXINGTON, Mass., May 04, 2021 (GLOBE NEWSWIRE) -- Kaleido Biosciences, Inc. (Nasdaq: KLDO), a clinical-stage healthcare company with a differentiated, chemistry-driven approach to targeting the microbiome to treat disease and improve human health, today reported financial results for the first quarter ended March 31, 2021.
“Kaleido is off to a strong start in 2021 marked by positive results from our 350-patient clinical study with KB109 in outpatients with mild-to-moderate COVID-19 and a recently completed financing, which will support the continued expansion of our novel, targeted Microbiome Metabolic TherapyTM (MMT) candidates,” said Dan Menichella, President and Chief Executive Officer of Kaleido. “Consistent with the interim findings we reported earlier this year, results from the full dataset demonstrated that KB109 has a favorable safety and tolerability profile and reduced COVID-19 related healthcare utilization and recovery time in patients with one or more comorbidity. Based on these results, we are investing in the manufacturing of KB109 and are initiating an IND application with the FDA.”
Continued Mr. Menichella: “Beyond our COVID-19 program, we have a robust pipeline of MMT-based candidates that holds immense potential. We continue to make progress enrolling patients in our non-IND study evaluating KB295 in individuals with mild-to-moderate ulcerative colitis with topline data anticipated mid-year. We believe these data are critical as patients and clinicians express interest in novel, oral therapeutic options with a strong safety and tolerability profile.”
Recent Program and Corporate Highlights
- An analysis from the full dataset (n=350) of the K031 controlled non-IND study of KB109 in patients with mild-to-moderate COVID-19 demonstrated a reduction in overall COVID-19 related healthcare utilization—comprised of hospitalizations, emergency room visits, and urgent care visits. The study also demonstrated a significant reduction in recovery time for patients age 45 and older or with one or more comorbidity who received KB109 plus self-supportive care as compared to patients receiving self-supportive care alone.
- In February, Kaleido closed a public offering with gross proceeds of approximately
$69.4 million , before deducting underwriting discounts and commissions and other offering expenses. - In April, Kaleido announced a research collaboration with researcher Robert Jenq, M.D. Professor of Genomic Medicine, at The University of Texas MD Anderson Cancer Center, to explore the potential of Kaleido’s novel MMT in preventing febrile neutropenia—a serious complication associated with hematopoietic stem cell transplantations (HSCT).
First Quarter Financial Results
Kaleido reported a net loss of
Research and development (R&D) expenses were
General and administrative (G&A) expenses were
As of March 31, 2021, the Company reported cash and cash equivalents of
About Microbiome Metabolic Therapies (MMT™)
Kaleido’s Microbiome Metabolic Therapies, or MMTs, are designed to drive the function and distribution of the microbiome’s existing microbes in order to decrease or increase the production of metabolites, or to advantage or disadvantage certain bacteria in the microbiome community. The Company’s initial MMT candidates are targeted, synthetic glycans that are orally administered, have limited systemic exposure, and are selectively metabolized by enzymes in the microbiome. Kaleido utilizes its discovery and development platform to study MMTs in microbiome samples to rapidly advance MMT candidates rapidly into clinical studies in healthy subjects and patients. These human clinical studies are conducted under regulations supporting research with food, evaluating safety, tolerability and potential markers of effect. For MMT candidates that are further developed as therapeutics, the Company conducts clinical trials under an Investigational New Drug (IND) or regulatory equivalent outside the U.S., and in Phase 2 or later development.
About Kaleido Biosciences
Kaleido Biosciences is a clinical-stage healthcare company with a differentiated, chemistry-driven approach to targeting the microbiome to treat disease and improve human health. The Company has built a proprietary product platform to enable the rapid and cost-efficient discovery and development of novel Microbiome Metabolic Therapies (MMT™). MMTs are designed to modulate the metabolic output and profile of the microbiome by driving the function and distribution of the gut’s existing microbes. Kaleido is advancing a broad pipeline of MMT candidates with the potential to address a variety of diseases and conditions with significant unmet patient needs. To learn more, visit https://kaleido.com/.
Forward-Looking Statements
This press release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, including, but not limited to, statements regarding the timing of initiation, completion and reporting of results of clinical studies, and our anticipated regulatory filings, strategy, business plans and focus. The use of words such as “may,” “might,” “will,” “should,” “expect,” “plan,” “anticipate,” “believe,” “estimate,” “project,” “intend,” “future,” “potential,” or “continue,” and other similar expressions are intended to identify such forward-looking statements. All such forward-looking statements are based on management's current expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties include fluctuations in our stock price, changes in market conditions and satisfaction of customary closing conditions related to the public offering and those risks more fully discussed in the section entitled "Risk Factors" in Kaleido’s annual report on Form 10-K for the fiscal year ended December 31, 2020, which is available at www.sec.gov, as well as discussions of potential risks, uncertainties, and other important factors in Kaleido’s subsequent filings with the Securities and Exchange Commission. Any forward-looking statements represent Kaleido’s views only as of today and should not be relied upon as representing its views as of any subsequent date. All information in this press release is as of the date of the release, and Kaleido undertakes no duty to update this information unless required by law.
Kaleido Biosciences, Inc. and Subsidiaries
Condensed Consolidated Statement of Operations (Unaudited)
(in thousands, except share and per share data)
Three Months Ended March 31, | ||||||||
2021 | 2020 | |||||||
Revenue: | ||||||||
Collaboration revenue | $ | 297 | $ | — | ||||
Operating expenses: | ||||||||
Research and development | 17,185 | 13,137 | ||||||
General and administrative | 5,460 | 5,917 | ||||||
Total operating expenses | 22,645 | 19,054 | ||||||
Loss from Operations | (22,348 | ) | (19,054 | ) | ||||
Other (expense) income | (694 | ) | (497 | ) | ||||
Net loss | $ | (23,042 | ) | $ | (19,551 | ) | ||
Net loss per share—basic and diluted | $ | (0.58 | ) | $ | (0.64 | ) | ||
Weighted-average common shares outstanding—basic and diluted | 39,692,582 | 30,333,283 |
Kaleido Biosciences, Inc. and Subsidiaries
Condensed Consolidated Balance Sheet Data (Unaudited)
(in thousands)
March 31, 2021 | December 31, 2020 | |||||||
Assets: | ||||||||
Cash and cash equivalents | $ | 92,362 | $ | 46,222 | ||||
Other assets | 12,664 | 13,122 | ||||||
Total assets | $ | 105,026 | $ | 59,344 | ||||
Liabilities and stockholders' equity | ||||||||
Liabilities | $ | 33,252 | $ | 38,848 | ||||
Stockholders' equity | 71,774 | 20,496 | ||||||
Total liabilities and stockholders' equity | $ | 105,026 | $ | 59,344 |
Contacts:
Kaleido Biosciences
William Duke, Jr.
Chief Financial Officer
617-890-5772
william.duke@kaleido.com
Investors
Mike Biega
Solebury Trout
617-221-9660
mbiega@soleburytrout.com
Media
Amy Bonanno
Solebury Trout
914-450-0349
abonanno@soleburytrout.com
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