Allena Pharmaceuticals Reports Fourth Quarter 2019 and Full Year 2019 Financial Results and Provides Business Update
-- Streamlined URIROX-2 Design Potentially Reduces Target Length and Cost of Trial --
-- Regulatory Engagement on Registrational Path for Reloxaliase in High-Risk Enteric Hyperoxaluria (EH) Patients with Chronic Kidney Disease (CKD) Expected in 2Q 2020 --
-- Investigational New Drug (IND) Application for ALLN-346 Receives Clearance to Proceed with First-in-Human Clinical Trial --
“The evolving COVID-19 pandemic has reminded us of the critical importance of medical innovation, and the value of both acute responsiveness to healthcare crises and the longer-term development of novel therapies to sustain and improve human health,” said
Recent Business Highlights and Upcoming Milestones:
Reloxaliase: Reloxaliase is a first-in-class, non-absorbed, orally administered enzyme for the treatment of severe hyperoxaluria. Allena is currently evaluating reloxaliase for patients with EH in URIROX-2, the second pivotal Phase 3 clinical trial in its URIROX program, and also plans to engage with the FDA in the second quarter of 2020 to explore a possible registration path for reloxaliase in patients with EH and advanced CKD.
- Reduction in the target enrollment to 200 subjects to support a potential Biologics License Application (BLA) filing for accelerated approval.
- The first sample size reassessment (SSR) based on total accrued KS events once 130 subjects have reached six months of treatment.
- Inclusion of a new sponsor-blinded estimation of the conditional probability of achieving the study’s primary and key secondary UOx endpoints at the time of the first SSR.
Allena expects to submit a protocol amendment and associated study documents for the revised trial design in the first quarter of 2020. Subject to Allena’s ability to secure additional financial resources and the impact of COVID-19 on its business, the first SSR is expected in the third quarter of 2021.
ALLN-346: ALLN-346 is a first-in-class, orally administered, novel urate degrading enzyme that has been designed for activity and stability in the gastrointestinal tract for the treatment of hyperuricemia in patients with gout in the setting of advanced CKD.
In the first quarter of 2020, Allena’s Investigational New Drug (IND) application for ALLN-346 received clearance from the FDA to proceed with first-in-human clinical trials. Subject to Allena’s ability to secure additional financial resources and the impact of COVID-19 on its business, Allena expects to initiate a Phase 1 clinical trial of ALLN-346 in the first half of 2020 and to report initial data from the trial in the fourth quarter of 2020.
Fourth Quarter and Full Year 2019 Financial Results:
- Cash Position: As of December 31, 2019, cash and cash equivalents were $30.0 million, as compared to $61.6 million as of December 31, 2018. This decrease was primarily due to cash used in operating activities, partially offset by
$12.0 millionof net proceeds from the issuance of common stock during 2019.
- R&D Expenses: R&D expenses were $8.7 million for the fourth quarter of 2019 and
$37.2 millionfor the year ended December 31, 2019, as compared to $7.3 million for the fourth quarter of 2018 and $26.4 millionfor the year ended December 31, 2018. This increase was primarily due to costs incurred for the URIROX-2 trial, which was initiated in the fourth quarter of 2018, an increase in formulation and development costs incurred advancing ALLN-346 to IND and an increase in employee-related costs. These costs were partially offset by a decrease of costs for the URIROX-1 trial, for which the company reported topline data in the fourth quarter of 2019.
- G&A Expenses: G&A expenses were $2.0 million for the fourth quarter of 2019 and
$9.7 millionfor the year ended December 31, 2019, as compared to $2.5 million for the fourth quarter of 2018 and $9.2 millionfor the year ended December 31, 2018. This increase was primarily due to an increase in employee compensation and benefit costs.
- Restructuring Charges: Allena incurred restructuring charges of
$0.6 millionfor the fourth quarter 2019 and for the year ended December 31, 2019due to a reduction of workforce completed in December 2019.
- Net Loss: Net loss was $11.4 million for the fourth quarter of 2019 and
$47.3 millionfor the year ended December 31, 2019, or a net loss per basic and diluted share of $0.47 and $2.13, respectively, as compared to a net loss of $9.6 million for the fourth quarter of 2018 and $35.6 millionfor the year ended December 31, 2018, or a net loss per basic and diluted share of $0.46 and $1.72, respectively.
This release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, including, without limitation, statements regarding the statements regarding the planned amended trial design for URIROX-2 and agreement in principle with the FDA about the amended design, the timing of sample size reassessments and interim analyses during the URIROX-2 trial, Allena’s ability to utilize the accelerated approval regulatory pathway for reloxaliase, statements concerning the future clinical, regulatory and commercial potential of reloxaliase, statements regarding the Allena’s development of ALLN-346, statements regarding Allena’s financial position and need for capital. The planned amended trial design for URIROX-2 will be subject to a protocol amendment and associated study documents, which Allena plans to submit to the FDA shortly, and additional modifications to URIROX-2 may be required, which modifications could be material. The FDA has advised Allena that, while it agrees in principle with the planned revisions to URIROX-2, certain details, to be specified in the protocol amendment and associated study documents for the revised trial design, remain subject to further clarification and confirmation with the FDA. In addition, it should be noted that additional capital will be required to complete the planned URIROX-2 clinical trial, which capital may not be available to Allena on terms that are acceptable to it, if at all. If adequate funds are not available on a timely basis, Allena may be required to delay, limit, reduce or terminate its clinical development of reloxaliase. The impact of the COVID-19 coronavirus on Allena’s business, the biotech sector generally and the broader macroeconomic environment is uncertain and could harm Allena’s business by delaying regulatory review timelines, clinical development plans and our ability to raise necessary capital. Furthermore, Allena does not have sufficient cash to operate its business for the next 12 months, which raises substantial doubt about its ability to continue as a going concern. Allena will require additional capital to fund its planned operations, which may not be available to it on attractive terms or at all. If the company is unable to secure additional capital, it will be forced to delay, limit, reduce or terminate its development of reloxaliase and may not be able to continue as a going concern. Any forward-looking statements in this press release 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, but are not limited to: the risk that the results of the URIROX-1 clinical trial may not be replicated in the URIROX-2 or other clinical trials of reloxaliase; the risk that the reduction in 24-hour UOx excretion observed in the placebo arm of the URIROX-1 trial may be observed in the URIROX-2 or other clinical trials of reloxaliase, which may have a negative impact on Allena’s ability to secure regulatory approval for this product candidate; the risk that results of earlier studies, or interim results, may not be predictive of future clinical trial results, and planned and ongoing studies may not establish an adequate safety or efficacy profile for reloxaliase to support regulatory approval or the use of the accelerated approval regulatory pathway; risks related to Allena’s ability to utilize the accelerated approval pathway for reloxaliase, including the risk that available data at the time of any sample size re-estimation or interim analysis conducted during the URIROX-2 trial may not be sufficient to demonstrate an increased probability of kidney stone events in patients with enteric hyperoxaluria and increasing UOx levels; the risk that the FDA may require that Allena increase the sample size or duration of treatment following the sample size reassessments to be conducted in accordance with the adaptive design element of the trial or otherwise collect additional clinical data from the URIROX-2 or other clinical trials prior to submitting a BLA for reloxaliase; risks associated with Allena’s ability to enroll a sufficient number of patients to adequately power URIROX-2 in order to achieve ultimate statistical success for kidney stone disease progression in the long-term follow-up phase of the trial; risks related to Allena’s use of UOx and/or POx as surrogate endpoints in its ongoing clinical trials, neither of which it believes have been previously utilized as biomarkers to support regulatory approval of other drug candidates, and the risks related to validating that reductions in UOx and/or POx correlate with meaningful clinical benefit; risks associated with obtaining, maintaining and protecting intellectual property; risks associated with Allena’s ability to enforce its patents against infringers and defend its patent portfolio against challenges from third parties; the risk of competition from other companies developing products for similar uses; risk associated with Allena’s financial condition and its need to obtain additional funding to support its business activities, including the future clinical development of reloxaliase and its ability to continue as a going concern; risks associated with Allena’s dependence on third parties; and risks related to the COVID-19 coronavirus. For a discussion of other risks and uncertainties, and other important factors, any of which could cause Allena’s actual results to differ from those contained in the forward-looking statements, see the section entitled “Risk Factors” in Item 1A of Part I of Allena’s Annual Report on Form 10-K for the year ended
|Selected Condensed Consolidated Balance Sheet Data|
|Cash and cash equivalents||$||30,007||$||61,643|
|Working capital (1)||22,127||58,706|
|Loan payable, net of current portion and discount||5,988||9,980|
|Total stockholders' equity||17,198||49,456|
|(1) The Company defines working capital as current assets less current liabilities. See the Company's condensed consolidated financial statements for further detail regarding its current assets and current liabilities.|
|Condensed Consolidated Statements of Operations|
|(in thousands, except share and per share data)|
|For the Three Months Ended
||For the Year Ended
|Research and development||$||8,721||$||7,269||$||37,244||$||26,376|
|General and administrative||1,967||2,511||9,676||9,217|
|Total operating expenses||11,293||9,780||47,525||35,593|
|Other income (expense), net||(66)||169||186||(55)|
|Net loss per share attributable to common
stockholders—basic and diluted
|Weighted-average common shares
outstanding—basic and diluted
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Source: Allena Pharmaceuticals, Inc.