ORIC® Pharmaceuticals Reports Fourth Quarter and Full Year 2024 Financial Results and Operational Updates
February 18 2025 - 3:05PM
ORIC Pharmaceuticals, Inc. (Nasdaq: ORIC), a clinical stage
oncology company focused on developing treatments that address
mechanisms of therapeutic resistance, today reported financial
results and operational updates for the quarter and year ended
December 31, 2024.
"2024 was a year of significant advancements
across several areas," stated Jacob M. Chacko, M.D., president and
chief executive officer. "Key achievements included initiation of
multiple cohorts for ORIC-114 in non-small cell lung cancer and
ORIC-944 in metastatic castration-resistant prostate cancer. We
also established three strategic partnerships with major
pharmaceutical companies, expanded our leadership team's expertise,
and secured $125 million in financing, which extends our cash
runway into late 2026. We anticipate seven data readouts in the
next year and a half and are working towards potential registration
studies for ORIC-114 in the latter half of 2025 and for ORIC-944 in
early 2026."
2024 Key Accomplishments
ORIC-114: a brain
penetrant, orally bioavailable, irreversible EGFR/HER2
inhibitor
- Entered into a clinical trial
collaboration and supply agreement with Johnson & Johnson to
evaluate ORIC-114 in combination with subcutaneous (SC) amivantamab
for the 1L treatment of patients with non-small cell lung cancer
(NSCLC) harboring EGFR exon 20 insertion mutations.
- Initiated a cohort to evaluate
ORIC-114 monotherapy for the 1L treatment of patients with NSCLC
harboring EGFR exon 20 insertion mutations.
- Announced the completion of the
dose escalation portion of the Phase 1b trial of ORIC-114 and the
selection of two provisional recommended phase 2 doses; after
which, initiated dosing of patients across three expansion cohorts
in the Phase 1b trial of ORIC-114 in patients with mutated NSCLC,
including 2L EGFR exon 20 insertion (EGFR exon 20 inhibitor naïve),
2L+ HER2 exon 20 insertion, and 2L+ EGFR atypical mutations.
- Presented preclinical data
demonstrating potential best-in-class properties, including potency
and selectivity, of ORIC-114 to treat NSCLC harboring EGFR exon 20
insertion mutations and other atypical EGFR mutations at the
EORTC-NCI-AACR Symposium on Molecular Targets and Cancer
Therapeutics.
ORIC-944: a potent and
selective allosteric inhibitor of PRC2
- Reported encouraging early safety
and efficacy data in ongoing dose escalation trial for ORIC-944 in
combination with apalutamide in patients with metastatic castration
resistant prostate cancer (mCRPC).
- Initiated dosing of ORIC-944 in
combination with ERLEADA® (apalutamide) and in combination with
NUBEQA® (darolutamide) in mid-2024 in the ongoing Phase 1b trial
for prostate cancer.
- Entered into clinical trial
collaboration and supply agreements with Johnson & Johnson and
Bayer to support the ongoing Phase 1b trial of ORIC-944 in
combination with AR inhibitors for the treatment of mCRPC.
- Reported initial Phase 1b single
agent data for ORIC-944 in metastatic prostate cancer supporting
advancement into combination development and demonstrating the
potential as a best-in-class PRC2 inhibitor, including a clinical
half-life of ~20 hours, robust target engagement, no signs of CYP
autoinduction that was observed with first-generation PRC2
inhibitors, and a generally well-tolerated safety profile.
- Presented preclinical data at the
2024 AACR Annual Meeting demonstrating superior drug properties and
synergy data in prostate cancer models, reinforcing the promise of
ORIC-944 as a potential best-in-class treatment for combination
with AR inhibitors.
Corporate Highlights:
- Strengthened cash position and
runway with a $125 million private placement financing from new and
existing healthcare specialist funds.
- Expanded the leadership team with
the appointment of industry veteran Keith Lui as Senior Vice
President of Commercial and Medical Affairs.
Anticipated Program
Milestones
ORIC anticipates the following upcoming
data milestones:
- ORIC-114 (NSCLC):
- 1H 2025: 2L EGFR exon 20 and 2L+ HER2 exon 20
- 2H 2025: 2L+ EGFR atypical
- 1H 2026: 1L EGFR exon 20
- Mid-2026: 1L EGFR exon 20 combination with SC amivantamab and
1L EGFR atypical
- ORIC-944 (mCRPC):
- 4Q 2025 / 1H 2026: Combination with AR inhibitors
Fourth Quarter and Full Year 2024
Financial Results
- Cash, Cash Equivalents and
Investments: Cash, cash equivalents and investments
totaled $256 million as of December 31, 2024, which is
expected to fund the current operating plan into late 2026.
- R&D
Expenses: Research and development (R&D) expenses
were $32.0 million for the three months ended December 31, 2024,
compared to $24.5 million for the three months ended December 31,
2023, an increase of $7.5 million. For the year ended December 31,
2024, R&D expenses were $114.1 million compared to $85.2
million for the same period in 2023, an increase of $28.9 million.
The increases were due to a net increase in external expenses
related to the advancement of product candidates, as well as higher
personnel costs, including additional non-cash stock-based
compensation.
- G&A
Expenses: General and administrative (G&A)
expenses were $7.6 million for the three months ended December
31, 2024, compared to $6.9 million for the three months ended
December 31, 2023, an increase of $0.7 million. For the year ended
December 31, 2024, G&A expenses were $28.8 million compared to
$25.6 million for the same period in 2023, an increase of $3.2
million. The increases were primarily due to higher personnel
costs, including additional non-cash stock-based compensation.
About ORIC Pharmaceuticals,
Inc. ORIC Pharmaceuticals is a clinical stage
biopharmaceutical company dedicated to improving patients’ lives
by Overcoming Resistance In Cancer. ORIC’s
clinical stage product candidates include (1) ORIC-114, a brain
penetrant inhibitor that selectively targets EGFR exon 20, HER2
exon 20 and EGFR atypical mutations, being developed across
multiple genetically defined cancers, and (2) ORIC-944, an
allosteric inhibitor of the polycomb repressive complex 2 (PRC2)
via the EED subunit, being developed for prostate cancer. Beyond
these two product candidates, ORIC® is also developing multiple
precision medicines targeting other hallmark cancer resistance
mechanisms. ORIC has offices in South San Francisco and San Diego,
California. For more information, please go
to www.oricpharma.com, and follow us on X or
LinkedIn.
Cautionary Note Regarding
Forward-Looking StatementsThis press release contains
forward-looking statements as that term is defined in Section 27A
of the Securities Act of 1933 and Section 21E of the Securities
Exchange Act of 1934. Statements in this press release that are not
purely historical are forward-looking statements. Such
forward-looking statements include, among other things, statements
regarding the continued clinical development of ORIC-114 and
ORIC-944; statements regarding the potential best-in-class
properties of ORIC-114 and ORIC-944; clinical outcomes, which may
materially change as patient enrollment continues or more patient
data become available; the development plans and timelines for
ORIC-114, ORIC-944 and ORIC’s other programs; the potential
advantages of ORIC-114, ORIC-944 and ORIC’s other programs; plans
underlying ORIC’s clinical trials and development; anticipated
program milestones, including timing of program and data updates
and the initiation of registrational studies; the period over which
ORIC estimates its existing cash, cash equivalents and investments
will be sufficient to fund its current operating plan; and
statements by the company’s chief executive officer. Words such as
“believes,” “anticipates,” “plans,” “expects,” “intends,” “will,”
“goal,” “potential” and similar expressions are intended to
identify forward-looking statements. The forward-looking statements
contained herein are based upon ORIC’s current expectations and
involve assumptions that may never materialize or may prove to be
incorrect. Actual results could differ materially from those
projected in any forward-looking statements due to numerous risks
and uncertainties, including but not limited to: risks associated
with the process of discovering, developing and commercializing
drugs that are safe and effective for use as human therapeutics and
operating as an early clinical stage company; ORIC’s ability to
develop, initiate or complete preclinical studies and clinical
trials for, obtain approvals for and commercialize any of its
product candidates; changes in ORIC’s plans to develop and
commercialize its product candidates; the potential for clinical
trials of ORIC’s product candidates to differ from preclinical,
initial, interim, preliminary or expected results; negative impacts
of health emergencies, economic instability or international
conflicts on ORIC’s operations, including clinical trials; the risk
of the occurrence of any event, change or other circumstance that
could give rise to the termination of ORIC’s license and
collaboration agreements or its clinical trial collaboration and
supply agreements; the potential market for ORIC’s product
candidates, and the progress and success of competing therapeutics
currently available or in development; ORIC’s ability to raise any
additional funding it will need to continue to pursue its business
and product development plans; regulatory developments in the
United States and foreign countries; ORIC’s reliance on third
parties, including contract manufacturers and contract research
organizations; ORIC’s ability to obtain and maintain intellectual
property protection for its product candidates; the loss of key
scientific or management personnel; competition in the industry in
which ORIC operates; general economic and market conditions; and
other risks. Information regarding the foregoing and additional
risks may be found in the section titled “Risk Factors” in ORIC’s
Annual Report on Form 10-K filed with the Securities and Exchange
Commission (the “SEC”) on February 18, 2025, and ORIC’s future
reports to be filed with the SEC. These forward-looking statements
are made as of the date of this press release, and ORIC assumes no
obligation to update the forward-looking statements, or to update
the reasons why actual results could differ from those projected in
the forward-looking statements, except as required by law.
Contact:Dominic Piscitelli,
Chief Financial
Officerdominic.piscitelli@oricpharma.cominfo@oricpharma.com
|
|
ORIC PHARMACEUTICALS, INC. CONDENSED BALANCE
SHEETS(in thousands, except share and per share
amounts) |
|
|
December 31, |
|
|
2024 |
|
|
2023 |
|
Assets |
|
Current assets: |
|
|
|
|
|
Cash, cash equivalents and short-term investments |
$ |
255,960 |
|
|
$ |
208,187 |
|
Prepaid expenses and other current assets |
|
6,290 |
|
|
|
4,410 |
|
Total current assets |
|
262,250 |
|
|
|
212,597 |
|
|
|
|
|
|
|
Long-term investments |
|
- |
|
|
|
26,852 |
|
Property and equipment, net |
|
2,924 |
|
|
|
2,862 |
|
Other assets |
|
8,968 |
|
|
|
9,696 |
|
Total assets |
$ |
274,142 |
|
|
$ |
252,007 |
|
|
|
|
|
|
|
Liabilities and Stockholders' Equity |
|
Current liabilities: |
|
|
|
|
|
Accounts payable |
$ |
1,548 |
|
|
$ |
944 |
|
Accrued liabilities |
|
23,298 |
|
|
|
19,514 |
|
Total current liabilities |
|
24,846 |
|
|
|
20,458 |
|
|
|
|
|
|
|
Other long-term liabilities |
|
6,174 |
|
|
|
7,461 |
|
Total liabilities |
|
31,020 |
|
|
|
27,919 |
|
|
|
|
|
|
|
Total stockholders'
equity |
|
243,122 |
|
|
|
224,088 |
|
Total liabilities and stockholders' equity |
$ |
274,142 |
|
|
$ |
252,007 |
|
|
ORIC PHARMACEUTICALS, INC.STATEMENTS OF OPERATIONS
AND COMPREHENSIVE LOSS(Unaudited)(in
thousands, except share and per share amounts) |
|
|
Three Months Ended December 31, |
|
|
Twelve Months Ended December 31, |
|
|
2024 |
|
|
2023 |
|
|
2024 |
|
|
2023 |
|
Operating expenses: |
|
|
|
|
|
|
|
|
|
|
|
Research and development |
$ |
31,970 |
|
|
$ |
24,481 |
|
|
$ |
114,072 |
|
|
$ |
85,172 |
|
General and administrative |
|
7,600 |
|
|
|
6,947 |
|
|
|
28,823 |
|
|
|
25,608 |
|
Total operating expenses |
|
39,570 |
|
|
|
31,428 |
|
|
|
142,895 |
|
|
|
110,780 |
|
Loss from operations |
|
(39,570 |
) |
|
|
(31,428 |
) |
|
|
(142,895 |
) |
|
|
(110,780 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
Other income, net |
|
3,263 |
|
|
|
3,098 |
|
|
|
15,048 |
|
|
|
10,083 |
|
Net loss |
$ |
(36,307 |
) |
|
$ |
(28,330 |
) |
|
$ |
(127,847 |
) |
|
$ |
(100,697 |
) |
Other comprehensive (loss)
income: |
|
|
|
|
|
|
|
|
|
|
|
Unrealized (loss) gain on investments |
|
(343 |
) |
|
|
627 |
|
|
|
121 |
|
|
|
1,549 |
|
Comprehensive loss |
$ |
(36,650 |
) |
|
$ |
(27,703 |
) |
|
$ |
(127,726 |
) |
|
$ |
(99,148 |
) |
Net loss per share, basic and
diluted |
$ |
(0.51 |
) |
|
$ |
(0.49 |
) |
|
$ |
(1.83 |
) |
|
$ |
(1.96 |
) |
Weighted-average shares
outstanding, basic and diluted |
|
70,652,013 |
|
|
|
57,464,041 |
|
|
|
69,727,940 |
|
|
|
51,450,848 |
|
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