Tricida Announces Third Quarter 2020 Financial Results
- As previously announced on
October 29, 2020, Tricidacompleted an End-of-Review Type A meeting with the FDA on October 20, 2020, that followed a Complete Response Letter (CRL) that was received by the company on August 21, 2020for the veverimer New Drug Application (NDA) that was under review by the U.S. Food and Drug Administration(FDA) through the Accelerated Approval Program. Based on feedback during the Type A meeting, Tricidanow believes the FDA will also require evidence of veverimer’s effect on CKD progression from a near-term interim analysis of the VALOR-CKD trial for approval under the Accelerated Approval Program and that the FDA is unlikely to rely solely on serum bicarbonate data for determination of efficacy. Prior to the End-of-Review Type A meeting, over nearly four years, Tricida’s discussions with the FDA focused on development of veverimer based solely on the use of serum bicarbonate as the surrogate endpoint to enable accelerated approval, with CKD progression data to be provided only at the completion of the VALOR-CKD trial. Tricidaplans to wait for formal meeting minutes from the FDA related to the End-of-Review Type A meeting prior to determining how to proceed with obtaining regulatory approval for veverimer. The company expects to receive the formal minutes within 30 days from the meeting.
- Announced a re-organization of the company following the End-of-Review Type A meeting to extend its financial runway in order to maximize the options for bringing veverimer to patients. In this re-organization, the company is reducing its headcount from 152 to 59 employees and is discussing its commitments with vendors and contract service providers to potentially provide additional financial flexibility. The reduction in headcount will reduce Tricida’s annual operating costs by approximately
- Continued to enroll patients in its ongoing VALOR-CKD trial. The trial has enrolled over 1,200 of its planned 1,600 subjects. Based on feedback received from FDA,
Tricidahas elected to focus future VALOR-CKD enrollment activities in the US, Canadaand 7 countries in Western Europe. It anticipates completing enrollment in the trial in 2022.
- Presented at the ASN Kidney Week 2020 Meeting real-world analyses from an Optum® de-identified Electronic Health Record dataset, 2007–2019, a longitudinal, clinical repository that includes 81 million de-identified patients from multiple large healthcare provider organizations across
the United States. Results of the analyses of patients with CKD and with and without metabolic acidosis showed that:
- Both baseline serum bicarbonate level and within-individual change in serum bicarbonate over time were significantly associated with differences in CKD progression as measured by time to ≥ 40% eGFR decline or progression by ≥ 1 CKD stage. Even small (1 mEq/L) increases in serum bicarbonate over time in patients with CKD were associated with significantly lower CKD progression rates.
- Metabolic acidosis was a significant independent predictor of all-cause mortality in patients with CKD.
- The presence of metabolic acidosis at baseline within every racial/ethnic group (Asian, Black, Hispanic, and non-Hispanic White) was independently associated with higher adjusted risk of death or adverse renal outcome.
- In patients with advanced CKD, metabolic acidosis was associated with an increased adjusted risk of progression to dialysis or kidney transplantation. This increased risk was independent of age, sex, race, pre-existing comorbidities, baseline eGFR, and baseline urine albumin to creatinine ratio (ACR).
- Presented at the ASN Kidney Week 2020 Meeting data from veverimer safety and efficacy and drug-drug interaction trials, including:
- New data describing the significant correlation between patient-reported limitations in daily activities as measured by the Kidney Disease Quality of Life – Physical Function Domain and objectively measured physical function using the 5-times repeated chair stand test.
- Evaluation of data from sub-populations of the 52-week TRCA-301/TRCA-301E trial, including elderly patients, diabetic patients, and female patients, showing similar results to the overall findings in this trial.
- Evaluation of safety data from the 52-week TRCA-301/TRCA-301E trial demonstrating that, consistent with its mechanism of action as an orally administered, non-absorbed, counterion-free polymer, veverimer caused no adverse effects on volume status or blood pressure in patients with CKD and metabolic acidosis.
- Data evaluating the potential for drug interactions with veverimer showing that veverimer had no effect on the bioavailability of drugs most susceptible to direct binding to the polymer. Veverimer caused modest, transient increases in gastric pH, but had no effect on the bioavailability of drugs with pH-sensitive solubility. The effect of veverimer on gastric pH is similar in the presence or absence of omeprazole.
Tricidaanticipates receipt of the formal minutes from the End-of-Review Type A meeting within 30 days from the meeting. Tricidaintends to provide a progress report to investors following receipt of the End-of-Review Type A meeting minutes to discuss the appropriate next steps toward its goal of obtaining FDA approval for veverimer.
“We believe the measures we have taken to re-organize our company will enable us to extend our operations to maximize our options to bring veverimer to patients,” said
Financial Results for the Three and Nine Months Ended
Research and development expense was
General and administrative expense was
Net loss was
For more information about
Cautionary Note on Forward-Looking Statements
This press release includes forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Forward-looking statements relate to expectations concerning matters that are not historical facts. Words such as “projects,” “believes,” “anticipates,” “plans,” “expects,” “intends,” “may,” “will,” “could,” “should,” “would,” and similar words and expressions are intended to identify forward-looking statements. These forward-looking statements include, but are not limited to, all of the statements under the heading “Upcoming Events” and other statements, including the Company’s plans and expectations with regard to its interactions and communications with the FDA, its plans and expectations as to the pathway to approval of veverimer by the FDA, including the potential availability of the Accelerated Approval Program, its plans and expectations for VALOR-CKD, and expectations regarding financial runway are forward-looking statements which involve risks and uncertainties that could cause actual results to differ materially from those discussed in such forward-looking statements. Such risks and uncertainties include, without limitation, the timing of the FDA’s approval of veverimer, if at all; the potential availability of the Accelerated Approval Program and the approvability of veverimer under that program; the Company’s plans and expectations with regard to its interactions with the FDA, including the potential resubmission of an NDA for veverimer; the Company’s plans and expectations for future clinical and product development milestones; the Company’s contractual and financial obligations to our key suppliers and vendors; the Company’s financial projections and cost estimates; and risks associated with the Company’s business prospects, financial results and business operations.
These and other factors that may affect the Company’s future business prospects, results and operations are identified and described in more detail in the Company’s filings with the
(Financial Tables to Follow)
Condensed Balance Sheets
|Cash and cash equivalents||$||29,712||$||18,574|
|Prepaid expenses and other current assets||8,063||4,744|
|Total current assets||326,059||312,742|
|Property and equipment, net||1,782||2,728|
|Operating lease right-of-use assets||14,204||9,376|
|Liabilities and stockholders’ equity|
|Current operating lease liabilities||1,822||1,072|
|Current Term Loan||13,714||—|
|Accrued expenses and other current liabilities||29,260||32,780|
|Total current liabilities||46,583||39,763|
|Non-current Term Loan, net||61,957||58,374|
|Convertible Senior Notes, net||116,625||—|
|Non-current operating lease liabilities||13,458||8,783|
|Other long-term liabilities||278||1,023|
|Additional paid-in capital||739,247||632,647|
|Accumulated other comprehensive income (loss)||432||193|
|Total stockholders’ equity||160,773||263,883|
|Total liabilities and stockholders’ equity||$||399,674||$||371,826|
Condensed Statements of Operations and Comprehensive Loss
(In thousands, except share and per share amounts)
|Three Months Ended
||Nine Months Ended
|Research and development||$||42,996||$||31,976||$||121,134||$||92,375|
|General and administrative||29,273||13,120||81,217||28,333|
|Total operating expenses||72,269||45,096||202,351||120,708|
|Loss from operations||(72,269||)||(45,096||)||(202,351||)||(120,708||)|
|Other income (expense), net||907||2,387||4,395||6,256|
|Loss before income taxes||(77,629||)||(44,119||)||(209,999||)||(118,642||)|
|Income tax benefit (expense)||(36||)||—||50||—|
|Other comprehensive income (loss):|
|Net unrealized gain (loss) on available-for-sale investments, net of tax||(431||)||(143||)||239||639|
|Total comprehensive loss||$||(78,096||)||$||(44,262||)||$||(209,710||)||$||(118,003||)|
|Net loss per share, basic and diluted||$||(1.55||)||$||(0.89||)||$||(4.20||)||$||(2.53||)|
|Weighted-average number of shares outstanding, basic and diluted||50,120,086||49,418,025||49,974,388||46,813,876|
GAAP to non-GAAP reconciliations
A reconciliation between net loss on a GAAP basis and on a non-GAAP basis is as follows:
|Three Months Ended
||Nine Months Ended
|GAAP net loss, as reported||$||(77,665||)||$||(44,119||)||$||(209,949||)||$||(118,642||)|
|Non-cash operating lease costs||207||233||597||646|
|Accretion of Term Loan and Convertible Senior Notes||2,915||553||5,246||1,564|
|Changes in fair value of compound derivative liability||(49||)||94||(699||)||259|
|Non-GAAP net loss||$||(64,277||)||$||(34,557||)||$||(177,037||)||$||(100,420||)|
Use of Non-GAAP Financial Measures
We supplement our financial statements presented on a GAAP basis by providing additional measures which may be considered “non-GAAP” financial measures under applicable
“Non-GAAP net loss” is not based on any standardized methodology prescribed by GAAP and represents GAAP net loss adjusted to exclude (1) non-cash operating lease costs, (2) accretion of Term Loan and Convertible Senior Notes, (3) stock-based compensation, (4) changes in fair value of compound derivative liability, and (5) restructuring costs, in reconciling of our GAAP to Non-GAAP net loss. Non-GAAP financial measures used by
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Source: Tricida, Inc.