Full Press Release Details
SERES THERAPEUTICS REPORTS FIRST QUARTER 2024 FINANCIAL RESULTS AND PROVIDES BUSINESS UPDATES
Continued market adoption of VOWST with approximately 1,411 patient enrollment
forms received, approximately 1,083 new patient starts, and net sales of $10.1 million during Q1 2024, and accelerated net sales in March and April
SER-155 Phase 1b placebo-controlled Cohort 2 clinical readout expected end of Q3 2024
Further microbiome therapeutic candidates have potential to expand product franchise into additional medically vulnerable patient populations
Conference call at 8:30 a.m. ET today
CAMBRIDGE, Mass. May 8, 2024 Seres Therapeutics, Inc. (Nasdaq: MCRB), a leading microbiome therapeutics company, today reported
first quarter 2024 financial results and provided business updates.
With a broad indication and compelling clinical profile to prevent the
recurrence of Clostridioides difficile infection (CDI) in adults following antibacterial treatment for recurrent CDI (rCDI), VOWST enables healthcare providers to fundamentally transform how they treat this life-threatening disease.
Along with our collaborators at Nestl Health Science, we have continued to make progress with the launch of VOWST. Nestl continues to refine its launch execution, and we have seen a resulting acceleration of VOWST sales during March
and April, said Eric Shaff, President and Chief Executive Officer of Seres.
Additionally, we completed enrollment of Cohort 2 in our ongoing SER-155 Phase 1b study and look forward to sharing a comprehensive topline dataset during the third quarter. These clinical results could further validate the vast potential of microbiome therapeutics in preventing
adverse outcomes linked to gastrointestinal pathogens, continued Mr. Shaff. Our goal remains to leverage Seres industry-leading microbiome capabilities to advance the development of
SER-155 and other product candidates in additional indications such as chronic liver disease, cancer neutropenia, and solid organ transplants, which could protect millions of medically vulnerable patients from
life-threatening infections. In support of this objective, we are evaluating various options to provide the Company with additional capital and to advance our pipeline.
VOWST Commercial Performance
Commercial adoption of VOWST has continued since its June 2023 launch in the U.S., with increasing breadth of utilization across healthcare providers. Metrics
are noted below as provided by Nestl Health Science:
Additional Program and Corporate Highlights
As of March 31, 2024, Seres had $111.2 million in cash and cash equivalents as compared with $128.0 million at the end of 2023. Based
on Seres current cash and various operating plans, the Company anticipates it has sufficient resources to support operations through obtaining the SER-155 Cohort 2 data and into the fourth quarter of
The Company s operating plans include drawing down the $45 million Tranche B under the Company s existing senior secured debt
facility with Oaktree Capital Management, L.P. if the net sales and other conditions are met, as well as alternate plans if such conditions are not met. Operating plans may include selling shares under the Company s at the market (ATM) equity
offering, implementing additional cost reduction initiatives, and other measures.
Conference Call Information
Seres management will host a conference call today, May 8, 2024, at 8:30 a.m. ET. The conference call may be accessed by calling 1-800-715-9871 (international callers dial 1-646-307-1963) and referencing the conference ID number 5686561. To join the live webcast, please visit the Investors and News section of the Seres website
at www.serestherapeutics.com. A webcast replay will be available on the Seres website beginning approximately two hours after the event and will be archived for at least 21 days.
INDICATION AND IMPORTANT SAFETY INFORMATION FOR VOWST
VOWST (fecal microbiota spores, live-brpk) is
indicated to prevent the recurrence of Clostridioides difficile infection (CDI) in individuals 18 years of age and older following antibacterial treatment for recurrent CDI (rCDI).
Limitation of Use: VOWST is not indicated for treatment of CDI.
IMPORTANT SAFETY INFORMATION
WARNINGS AND PRECAUTIONS
Transmissible infectious agents: Because VOWST is manufactured from human fecal matter, it may carry a risk of transmitting infectious
agents. Report any infection that is suspected to have been transmitted by VOWST to Aimmune Therapeutics, Inc. at
presence of food allergens: VOWST may contain food allergens. The potential to cause adverse reactions due to food allergens is unknown.
The most common adverse reactions (reported in 5% of participants) were abdominal distension (31.1%), fatigue (22.2%), constipation (14.4%), chills
(11.1%), and diarrhea (10.0%).
To report SUSPECTED ADVERSE REACTIONS, contact Aimmune Therapeutics at 1-833-AIM-2KNO (1-833-246-2566), or the FDA at 1-800-FDA-1088, or visit www.fda.gov/MedWatch.
Do not administer antibacterials
concurrently with VOWST.
Please see Full Prescribing Information and Patient Information
About Seres Therapeutics
Seres Therapeutics, Inc. (Nasdaq:
MCRB) is a commercial-stage company developing novel microbiome therapeutics for serious diseases. Seres lead program, VOWST , obtained U.S. FDA approval in April 2023 as the first
orally administered microbiome therapeutic to prevent recurrence of C. difficile infection (CDI) in adults following antibacterial treatment for recurrent CDI and is being commercialized in collaboration with Nestl Health
Science. Seres is evaluating SER-155 in a Phase 1b study in patients receiving allogeneic hematopoietic stem cell transplantation. For more information, please visit www.serestherapeutics.com.
Forward-Looking Statements
This press release contains
forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements,
including statements about the potential for VOWST; the timing and results of our clinical studies; future product candidates and development plans; our ability to generate additional capital; operating plans and the sufficiency of cash to fund
operations; and other statements which are not historical fact.
These forward-looking statements are based on management s current expectations.
These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results,
performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, the following: we have incurred significant losses, are not currently profitable and may never become profitable; our need for
additional funding; our history of operating losses; the restrictions in our debt agreement; the ability of our restructuring plan to deliver cash savings; our novel approach to therapeutic intervention; our reliance on third parties to conduct our
clinical trials and manufacture our product candidates; the competition we will face; our ability to protect our intellectual property; and our ability to retain key personnel and to manage our growth. These and other important factors discussed
under the caption Risk Factors in our Annual Report on Form 10-K filed with the Securities and Exchange Commission (SEC), on March 5, 2024, and our other reports filed with the SEC could cause
actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management s estimates as of the date of this press release. While we may elect
to update such forward-looking statements at some point in the future, we disclaim any obligation to do so, even if subsequent events cause our views to change. These forward-looking statements should not be relied upon as representing our views as
of any date subsequent to the date of this press release.
SERES THERAPEUTICS, INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
(unaudited, in thousands, except share and per share data)
| March 31, 2024 | December 31, 2023 | |||||||
| Assets | ||||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 111,184 | $ | 127,965 | ||||
| Collaboration receivable - related party | 7,418 | 8,674 | ||||||
| Inventories | 41,973 | 29,647 | ||||||
| Prepaid expenses and other current assets | 4,606 | 9,124 | ||||||
| Total current assets | 165,181 | 175,410 | ||||||
| Property and equipment, net | 19,115 | 22,457 | ||||||
| Operating lease assets | 105,669 | 109,793 | ||||||
| Restricted cash | 8,430 | 8,185 | ||||||
| Restricted investments | 1,401 | 1,401 | ||||||
| Other non-current assets (1) | 41,466 | 41,354 | ||||||
| Total assets | $ | 341,262 | $ | 358,600 | ||||
| Liabilities and Stockholders Deficit | ||||||||
| Current liabilities: | ||||||||
| Accounts payable | $ | 5,219 | $ | 3,641 | ||||
| Accrued expenses and other current liabilities (2) | 76,317 | 80,611 | ||||||
| Operating lease liabilities | 8,833 | 6,677 | ||||||
| Deferred income - related party | 8,109 | 7,730 | ||||||
| Total current liabilities | 98,478 | 98,659 | ||||||
| Long term portion of note payable, net of discount | 102,009 | 101,544 | ||||||
| Operating lease liabilities, net of current portion | 103,341 | 105,715 | ||||||
| Deferred revenue - related party | 95,364 | 95,364 | ||||||
| Warrant liabilities | 130 | 546 | ||||||
| Other long-term liabilities | 1,678 | 1,628 | ||||||
| Total liabilities | 401,000 | 403,456 | ||||||
| Commitments and contingencies (Note 15) | ||||||||
| Stockholders deficit: | ||||||||
| Preferred stock, $0.001 par value; 10,000,000 shares authorized at March 31, 2024 and December 31, 2023; no shares issued and outstanding at March 31, 2024 and December 31, 2023 | ||||||||
| Common stock, $0.001 par value; 240,000,000 shares authorized at March 31, 2024 and December 31, 2023, respectively; 151,442,034 and 135,041,467 shares issued and outstanding at March 31, 2024 and December 31, 2023, respectively | 151 | 135 | ||||||
| Additional paid-in capital | 958,479 | 933,244 | ||||||
| Accumulated other comprehensive loss | ||||||||
| Accumulated deficit | (1,018,368 | ) | (978,235 | ) | ||||
| Total stockholders deficit | (59,738 | ) | (44,856 | ) | ||||
| Total liabilities and stockholders deficit | $ | 341,262 | $ | 358,600 |
SERES THERAPEUTICS, INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
(unaudited, in thousands, except share and per share data)
| Three Months Ended March 31, | ||||||||
| 2024 | 2023 | |||||||
| Revenue: | ||||||||
| Collaboration revenue - related party | $ | $ | (522 | ) | ||||
| Total revenue | (522 | ) | ||||||
| Operating expenses: | ||||||||
| Research and development expenses | 21,702 | 43,969 | ||||||
| General and administrative expenses | 15,466 | 22,470 | ||||||
| Collaboration (profit) loss sharing - related party | 2,418 | 3,607 | ||||||
| Total operating expenses | 39,586 | 70,046 | ||||||
| Loss from operations | (39,586 | ) | (70,568 | ) | ||||
| Other income (expense): | ||||||||
| Interest income | 1,648 | 1,032 | ||||||
| Interest expense | (4,663 | ) | (1,948 | ) | ||||
| Other income | 2,468 | 310 | ||||||
| Total other expense, net | (547 | ) | (606 | ) | ||||
| Net loss | $ | (40,133 | ) | $ | (71,174 | ) | ||
| Net loss per share attributable to common stockholders, basic and diluted | $ | (0.27 | ) | $ | (0.57 | ) | ||
| Weighted average common shares outstanding, basic and diluted | 146,101,581 | 125,862,975 | ||||||
| Other comprehensive income (loss): | ||||||||
| Unrealized gain (loss) on investments, net of tax of $0 | 12 | |||||||
| Currency translation adjustment | 2 | |||||||
| Total other comprehensive income (loss) | 14 | |||||||
| Comprehensive loss | $ | (40,133 | ) | $ | (71,160 | ) |
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