Catabasis Pharmaceuticals Reports Fourth Quarter and Full Year 2017 Financial Results and Reviews Business Progress
-- Preparations Underway for Phase 3 Trial Following Positive Data Showing Substantially Slowed Duchenne Muscular Dystrophy Disease Progression Through More than One Year of Edasalonexent Treatment --
-- Plan to Initiate Phase 1 Trial for CAT-5571, a Potential Treatment for Cystic Fibrosis, Based on Preclinical Data Showing Potential of CAT-5571 to Clear Pathogens --
“We achieved several important clinical milestones in 2017 as we work
toward our vision of improving the lives of those affected by rare
diseases,” said
Recent and Upcoming Corporate Highlights
Edasalonexent (CAT-1004) for the Treatment of Duchenne Muscular
Dystrophy (DMD)
Consistent and sustained disease-modifying
effects of edasalonexent following 48 and 60 weeks of treatment in boys
with DMD were reported at the
- Preservation of muscle function and substantially slowed DMD disease progression compared to the pre-specified control period was observed through more than a year of edasalonexent treatment. Consistent improvements in all assessments of muscle function were observed following 48 and 60 weeks of oral 100 mg/kg/day edasalonexent treatment compared to the rates of change in the control period for boys prior to receiving edasalonexent treatment.
- Statistically significant changes from baseline in multiple non-effort based biomarkers of muscle health were seen.
- Edasalonexent continued to be well tolerated with no safety signals observed.
Additional data on edasalonexent were presented this week at the 2018
- Height and weight growth following 48 and 60 weeks of edasalonexent treatment was age-appropriate and on track with standard growth curves for unaffected boys in the same age range. Body mass index (BMI) trended towards a decrease. This profile is favorably differentiated from the typical profile associated with the corticosteroid standard of care in DMD which includes weight gain and curtailed growth.
- Heart rate data from boys treated with edasalonexent decreased toward age-normative values through 48 weeks of treatment. Cardiac failure is a leading cause of mortality in DMD. In the 4-7 year old age range, boys typically have resting tachycardia, a heart rate that exceeds the normal resting rate, which is the first cardiac manifestation in DMD.
Also presented at the 2018
- The ImagingDMD study annually assessed timed function tests, and a subset analysis was presented of 28 boys initially aged 5 to 8.5 years old at times when they were not taking corticosteroids. The timed function tests performed in the study were the same as those assessed in the MoveDMD trial, which was conducted at ImagingDMD sites.
- The observations in the ImagingDMD natural history study were generally consistent with the absolute functional abilities as well as declines in abilities experienced by boys in the off-treatment control period of the Catabasis MoveDMD trial. These data provide important corroboration that the MoveDMD off-treatment control period observations are characteristic of the expected natural history and provide added confidence in the slowing of disease progression treatment effects observed with edasalonexent.
Catabasis plans to initiate a global Phase 3 trial with edasalonexent in patients with DMD regardless of mutation type in the first half of 2018 with top-line results expected in 2020, dependent on raising capital.
CAT-5571 for the Treatment of Cystic Fibrosis (CF)
Data
demonstrating CAT-5571 improved cellular clearance of bacteria in
preclinical models of CF were presented at the
Catabasis expects to initiate a Phase 1 trial for CAT-5571 in the second half of 2018 and report top-line results in 2019, based on our current operating plan. This is supported by preclinical data showing CAT-5571 enhances the clearance of multiple types of pathogens.
Fourth Quarter and Full Year 2017 Financial Results
Cash Position: As of
R&D Expenses: Research and development expenses were
G&A Expenses: General and administrative expenses were
Operating Loss: Loss from operations was
Net Loss: Net loss was
Conference Call and Webcast
Catabasis will host a conference
call and webcast at 4:30pm ET today to provide an update on corporate
developments and to discuss fourth quarter and full year 2017 financial
results.
Participant Toll-Free Dial-In Number: | (877) 388-2733 | |||
Participant International Dial-In Number: | (541) 797-2984 | |||
Pass Code: | 7693708 | |||
Please specify to the operator that you would like to join the “Catabasis Fourth Quarter and Full Year 2017 Results Call.”
Interested parties may access a live audio webcast of the conference call via the investor section of the Catabasis website, www.catabasis.com. Please connect to the Catabasis website several minutes prior to the start of the broadcast to ensure adequate time for any software download that may be necessary. The webcast will be archived for 90 days.
About Edasalonexent (CAT-1004)
Edasalonexent (CAT-1004) is
an investigational oral small molecule that is being developed as a
potential disease-modifying therapy for all patients affected by DMD,
regardless of their underlying mutation. Edasalonexent inhibits NF-kB, a
protein that is activated in DMD and drives inflammation and fibrosis,
muscle degeneration and suppresses muscle regeneration. Edasalonexent
continues to be dosed in the open-label extension of the MoveDMD Phase 2
clinical trial and Catabasis plans to initiate a single global Phase 3
trial to evaluate the efficacy and safety of edasalonexent for
registration purposes in the first half of 2018, dependent on raising
capital. The
About CAT-5571
CAT-5571 is an investigational oral small
molecule designed to restore host defense by activating autophagy that
is being developed for the treatment of cystic fibrosis (CF). Autophagy
is a mechanism for recycling cellular components and digesting
pathogens, which is depressed in CF. People with CF suffer from
persistent lung infections with opportunistic pathogens such as Pseudomonas
aeruginosa and Burkholderia cenocepacia, causing
chronic infections that are difficult to eradicate and lead to
respiratory failure. CAT-5571 has been shown to restore autophagy,
reestablish host defense and enhance the clearance of pathogens,
including P. aeruginosa and B. cenocepacia, in preclinical
models of CF. CAT-5571 has the potential to augment the efficacy of
antibiotics and could also be used with other CF therapies, including
transmembrane conductance receptor (CFTR) targeted agents.
About Catabasis
At
Forward Looking Statements
Any statements in this press
release about future expectations, plans and prospects for the Company,
including statements about future clinical trial plans including, among
other things, statements about the Company’s plans to commence a single
global Phase 3 trial in DMD in the first half of 2018 to evaluate the
efficacy and safety of edasalonexent for registration purposes, the
Company’s plans to report top-line results from this trial in 2020, the
Company’s plans to initiate a Phase 1 trial for CAT-5571 in the second
half of 2018 and report top-line results in 2019 and the Company’s
expectation that its current operating plan provides for cash to fund
operations through
Catabasis Pharmaceuticals, Inc. |
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Condensed Consolidated Statements of Operations |
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(In thousands, except share and per share data) |
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(Unaudited) |
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Three Months Ended December 30, | Year Ended December 31, | |||||||||||
2017 | 2016 | 2017 | 2016 | |||||||||
Revenue | $ | 250 | $ | - | $ | 500 | $ | - | ||||
Operating expenses: | ||||||||||||
Research and development | 3,989 | 6,260 | 18,682 | 25,450 | ||||||||
General and administrative | 1,723 | 2,413 | 8,912 | 10,108 | ||||||||
Total operating expenses | 5,712 | 8,673 | 27,594 | 35,558 | ||||||||
Loss from operations | (5,462) | (8,673) | (27,094) | (35,558) | ||||||||
Other (expense) income: | ||||||||||||
Interest expense | (81) | (175) | (462) | (837) | ||||||||
Interest and investment income | 32 | 59 | 160 | 242 | ||||||||
Other income, net | 14 | 11 | 32 | 93 | ||||||||
Total other expense, net | (35) | (105) | (270) | (502) | ||||||||
Net loss | $ | (5,497) | $ | (8,778) | $ | (27,364) | $ | (36,060) | ||||
Net loss per share - basic and diluted | $ | (0.24) | $ | (0.47) | $ | (1.26) | $ | (2.22) | ||||
Weighted-average common shares outstanding used in net loss per share - basic and diluted | 23,218,476 | 18,699,480 | 21,681,534 | 16,230,190 | ||||||||
Catabasis Pharmaceuticals, Inc. Condensed Consolidated Balance Sheets (In thousands) (Unaudited) |
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As of December 31, | ||||||||||
2017 | 2016 | |||||||||
Assets | ||||||||||
Cash and cash equivalents | $ | 16,369 | $ | 23,596 | ||||||
Available-for-sale securities | - | 14,931 | ||||||||
Total assets | 17,897 | 40,209 | ||||||||
Liabilities and stockholders’ equity | ||||||||||
Current portion of notes payable, net of discount | 2,479 | 3,243 | ||||||||
Notes payable, net of current portion and discount | - | 2,479 | ||||||||
Total liabilities | 6,105 | 11,123 | ||||||||
Total stockholders’ equity | $ | 11,792 | $ | 29,086 | ||||||
Catabasis Pharmaceuticals, Inc. Condensed Consolidated Statements of Cash Flows (In thousands) (Unaudited) |
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Year Ended December 31, | ||||||||||||
2017 | 2016 | |||||||||||
Net cash used in operating activities | $ | (26,836 | ) | $ | (32,858 | ) | ||||||
Net cash provided by (used in) investing activities | 14,883 | (15,490 | ) | |||||||||
Net cash provided by financing activities | 4,726 | 9,164 | ||||||||||
Net decrease in cash and cash equivalents | $ | (7,227 | ) | $ | (39,184 | ) | ||||||
View source version on businesswire.com: http://www.businesswire.com/news/home/20180315005852/en/
Source:
Investor and Media Contact
Catabasis
Pharmaceuticals, Inc.
Andrea Matthews, 617-349-1971
amatthews@catabasis.com