Seres Therapeutics Reports Third Quarter Financial Results and Provides Business Update
– Two late-stage microbiome clinical study readouts in ulcerative colitis and C. difficile infection anticipated in 2020 –
– Debt facility secured, providing up to
– Conference call at
“Seres continues to advance our microbiome programs, and the Company is well resourced to reach important corporate milestones in 2020, including two late-stage clinical readouts: SER-287 Phase 2b study in mild-to-moderate ulcerative colitis and SER-109 Phase 3 study in recurrent C. difficile infection,” said
Program Updates and Corporate Highlights
-
SER-287 Phase 2b ECO-RESET study in ulcerative colitis: SER-287 is an orally-administered, biologically-derived, live microbiome therapeutic candidate designed to modulate the gastrointestinal microbiome of individuals with ulcerative colitis. Seres continues to enroll the SER-287 Phase 2b ECO-RESET induction study in patients with active mild-to-moderate ulcerative colitis. The SER-287 Phase 2b ECO-RESET study is expected to enroll approximately 201 patients. Based on
U.S. Food and Drug Administration feedback, Seres expects that with positive Phase 2b study results, the study could serve as one of two pivotal trials to enable a SER-287 Biologics License Application submission. Seres expects Phase 2b ECO-RESET study top-line results in the second half of 2020.
-
SER-109 Phase 3 ECOSPOR III study in recurrent C. difficile infection: SER-109 is an orally-administered, biologically-derived, live microbiome therapeutic candidate designed to restore the depleted, or dysbiotic, gastrointestinal microbiome of patients with recurrent C. difficile infection. The Company continues to enroll the ECOSPOR III trial, which is evaluating efficacy and safety in 188 patients with recurrent C. difficile infection. All patients enrolled in ECOSPOR III are required to test positive for C. difficile cytotoxin to ensure enrollment of only patients with an active C. difficile infection. As of
October 31 , ECOSPOR III was more than 85% enrolled, and top-line study results are expected in mid-2020.
-
SER-301 preclinical candidate for ulcerative colitis: The Company has nominated the lead candidate for SER-301, a rationally-designed, live microbiome therapeutic for ulcerative colitis. Next-generation, rationally-designed microbiome therapeutics may provide important benefits that include the optimization of pharmacological properties for target diseases and streamlined manufacturing. The consortia of bacteria in SER-301 are designed to modify the microbiome and microbe-associated metabolites in the gastrointestinal tract to modulate ulcerative colitis-relevant anti-inflammatory and immune pathways and to improve epithelial barrier integrity. SER-301 incorporates species associated with clinical efficacy in prior Seres human studies. Further, bacterial species selected for inclusion in SER-301 have been confirmed to engraft across human subjects. The consortia has demonstrated the capacity to modulate disease-relevant cellular mechanisms in human cell-based screening assays and in vivo models. Seres is entitled to a
$10 million milestone payment associated with the SER-301 Phase 1 clinical study from its ongoing collaboration with Nestlé Health Science. Seres expects to initiate clinical development in early 2020.
-
SER-401 Phase 1b in metastatic melanoma: SER-401 is an orally-administered, biologically-derived, live microbiome therapeutic candidate comprising bacteria that reflect the bacterial signature in the gastrointestinal microbiome associated with response to checkpoint inhibitor immunotherapy. The ongoing Phase 1b study, supported by the
Parker Institute for Cancer Immunotherapy andThe University of Texas MD Anderson Cancer Center , will evaluate the potential for SER-401 to improve clinical response to nivolumab, an approved anti-PD-1 checkpoint inhibitor therapy, and will evaluate tumor biopsies and various biomarkers. Seres expects to obtain SER-401 Phase 1b preliminary study results in the second half of 2020.
-
New debt financing: Seres entered into a debt financing agreement with
Hercules Capital inOctober 2019 that provides the Company with up to$50 million in additional capital. The Company received a first tranche of approximately$25 million following the agreement closing. Two subsequent tranches of$12.5 million each would become available to the Company upon the achievement of certain milestones.
Financial Results
Seres reported a net loss of
Research and development expenses for the third quarter of 2019 were
General and administrative expenses for the third quarter of 2019 were
Seres ended the third quarter with approximately
Cash resources are expected to fund operating expenses and capital expenditure requirements, excluding net cash flows from future business development activities or potential incoming milestone payments, into the second quarter of 2021.
Conference Call Information
Seres’ management will host a conference call today,
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.
About
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 the timing, results and initiation of our clinical studies, the potential for any of the Company’s studies to serve as a pivotal trial to enable a BLA submission, the receipt of future milestone payments, the potential impact of any of Seres’ development candidates, the sufficiency of the Company’s cash resources to fund operating expenses and capital expenditure requirements, the availability of additional cash resources and other statements that are not historical facts.
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 limited operating history; our unproven approach to therapeutic intervention; the lengthy, expensive and uncertain process of clinical drug development; our reliance on third parties and collaborators to conduct our clinical trials, manufacture our product candidates and develop and commercialize our product candidates, if approved; the success of our leadership transition; our ability to retain key personnel and to manage our growth; and our management and principal stockholders have the ability to control or significantly influence our business. These and other important factors discussed under the caption “Risk Factors” in our Annual Report on Form 10-Q filed with the
SERES THERAPEUTICS, INC.
|
||||||||
|
|
September 30, |
|
|
December 31, |
|
||
|
|
2019 |
|
|
2018 |
|
||
Assets |
|
|
|
|
|
|
|
|
Current assets: |
|
|
|
|
|
|
|
|
Cash and cash equivalents |
|
$ |
49,296 |
|
|
$ |
85,820 |
|
Investments |
|
|
34,492 |
|
|
|
— |
|
Prepaid expenses and other current assets |
|
|
4,073 |
|
|
|
6,845 |
|
Accounts receivable |
|
|
1,717 |
|
|
|
— |
|
Total current assets |
|
|
89,578 |
|
|
|
92,665 |
|
Property and equipment, net |
|
|
21,160 |
|
|
|
26,294 |
|
Operating lease assets |
|
|
11,899 |
|
|
|
— |
|
Restricted investments |
|
|
1,400 |
|
|
|
1,400 |
|
Restricted cash |
|
|
114 |
|
|
|
113 |
|
Total assets |
|
$ |
124,151 |
|
|
$ |
120,472 |
|
Liabilities and Stockholders’ Deficit |
|
|
|
|
|
|
|
|
Current liabilities: |
|
|
|
|
|
|
|
|
Accounts payable |
|
$ |
4,455 |
|
|
$ |
6,415 |
|
Accrued expenses and other current liabilities |
|
|
10,522 |
|
|
|
15,207 |
|
Operating lease liabilities |
|
|
4,335 |
|
|
|
— |
|
Deferred revenue - related party |
|
|
21,135 |
|
|
|
20,419 |
|
Deferred revenue |
|
|
1,790 |
|
|
|
— |
|
Total current liabilities |
|
|
42,237 |
|
|
|
42,041 |
|
Operating lease liabilities, net of current portion |
|
|
16,844 |
|
|
|
— |
|
Lease incentive obligation, net of current portion |
|
|
— |
|
|
|
6,776 |
|
Deferred rent |
|
|
— |
|
|
|
2,216 |
|
Deferred revenue, net of current portion - related party |
|
|
94,215 |
|
|
|
116,840 |
|
Deferred revenue, net of current portion |
|
|
2,410 |
|
|
|
— |
|
Other long-term liabilities |
|
|
664 |
|
|
|
644 |
|
Total liabilities |
|
|
156,370 |
|
|
|
168,517 |
|
Commitments and contingencies |
|
|
|
|
|
|
|
|
Stockholders’ deficit: |
|
|
|
|
|
|
|
|
Preferred stock, $0.001 par value; 10,000,000 shares authorized at September 30, 2019 and December 31, 2018; no shares issued and outstanding at September 30, 2019 and December 31, 2018 |
|
|
— |
|
|
|
— |
|
Common stock, $0.001 par value; 200,000,000 shares authorized at September 30, 2019 and December 31, 2018; 69,993,952 and 40,936,735 shares issued and outstanding at September 30, 2019 and December 31, 2018, respectively |
|
|
70 |
|
|
|
41 |
|
Additional paid-in capital |
|
|
408,575 |
|
|
|
341,284 |
|
Accumulated other comprehensive loss |
|
|
7 |
|
|
|
— |
|
Accumulated deficit |
|
|
(440,871 |
) |
|
|
(389,370 |
) |
Total stockholders’ deficit |
|
|
(32,219 |
) |
|
|
(48,045 |
) |
Total liabilities and stockholders’ deficit |
|
$ |
124,151 |
|
|
$ |
120,472 |
|
SERES THERAPEUTICS, INC.
|
||||||||||||||||
|
Three Months Ended September 30, |
|
|
Nine Months Ended September 30, |
|
|||||||||||
|
2019 |
|
|
2018 |
|
|
2019 |
|
|
2018 |
|
|||||
Revenue: |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Collaboration revenue - related party |
$ |
4,840 |
|
|
$ |
8,684 |
|
|
$ |
21,909 |
|
|
$ |
16,721 |
|
|
Grant revenue |
|
85 |
|
|
|
371 |
|
|
|
791 |
|
|
|
917 |
|
|
Collaboration revenue |
|
2,106 |
|
|
|
— |
|
|
|
4,183 |
|
|
|
— |
|
|
Total revenue |
|
7,031 |
|
|
|
9,055 |
|
|
|
26,883 |
|
|
|
17,638 |
|
|
Operating expenses: |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Research and development expenses |
|
18,317 |
|
|
|
23,675 |
|
|
|
59,109 |
|
|
|
71,188 |
|
|
General and administrative expenses |
|
5,897 |
|
|
|
7,591 |
|
|
|
18,966 |
|
|
|
25,063 |
|
|
Restructuring expenses |
|
— |
|
|
|
— |
|
|
|
1,492 |
|
|
|
— |
|
|
Total operating expenses |
|
24,214 |
|
|
|
31,266 |
|
|
|
79,567 |
|
|
|
96,251 |
|
|
Loss from operations |
|
(17,183 |
) |
|
|
(22,211 |
) |
|
|
(52,684 |
) |
|
|
(78,613 |
) |
|
Other income (expense): |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Interest income (expense), net |
|
335 |
|
|
|
262 |
|
|
|
744 |
|
|
|
958 |
|
|
Other income |
|
439 |
|
|
|
— |
|
|
|
439 |
|
|
|
— |
|
|
Total other income (expense), net |
|
774 |
|
|
|
262 |
|
|
|
1,183 |
|
|
|
958 |
|
|
Net loss |
$ |
(16,409 |
) |
|
$ |
(21,949 |
) |
|
$ |
(51,501 |
) |
|
$ |
(77,655 |
) |
|
Net loss per share attributable to common stockholders, basic and diluted |
$ |
(0.23 |
) |
|
$ |
(0.54 |
) |
|
$ |
(0.99 |
) |
|
$ |
(1.91 |
) |
|
Weighted average common shares outstanding, basic and diluted |
|
69,944,068 |
|
|
|
40,806,413 |
|
|
|
52,143,492 |
|
|
|
40,699,422 |
|
|
Net loss |
|
(16,409 |
) |
|
|
(21,949 |
) |
|
|
(51,501 |
) |
|
|
(77,655 |
) |
|
Other comprehensive income: |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Unrealized gain on investments, net of tax of $0 |
$ |
7 |
|
|
$ |
20 |
|
|
$ |
7 |
|
|
$ |
137 |
|
|
Total other comprehensive income |
|
7 |
|
|
|
20 |
|
|
|
7 |
|
|
|
137 |
|
|
Comprehensive loss |
$ |
(16,402 |
) |
|
$ |
(21,929 |
) |
|
$ |
(51,494 |
) |
|
$ |
(77,518 |
) |
View source version on businesswire.com: https://www.businesswire.com/news/home/20191105005223/en/
Source:
Seres Therapetics Contact
Carlo Tanzi, Ph.D.
Investor Relations
ctanzi@serestherapeutics.com