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ORIC Pharmaceuticals, Inc. (ORIC) SEC Filings & Earnings Calls

EquiReason read 16 ORIC Pharmaceuticals, Inc. SEC filings in the last 12 months. Latest: 8-K on 2026-10-23 — ORIC presented enozertinib (ORIC-114) program update at ESMO 2026, highlighting potential best-in-class profile in 1L EGFR atypical NSCLC, a >$2.5bn market, supporting rapid advanc.

Source: SEC EDGAR filings · figures as of 2026-06-30 · read by EquiReason

ORICORIC Pharmaceuticals, Inc.Follow ORIC — free
Biotechnology · Healthcare
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Next earnings
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Every filing, read

last 12 months · SEC

What happened, the numbers inside, guidance and risks. The original is one click away.

23 Oct 20268-K · 7.01, 8.01ORIC presented enozertinib (ORIC-114) program update at ESMO 2026, highlighting potential best-in-class profile in 1L EGFR atypical NSCLC, a >$2.5bn market, supporting rapid advancement to Phase 3.open

Risks flagged

Clinical trial risks and regulatory uncertainties remain; forward-looking statements highlight potential changes in outcomes as more data becomes available.

“Forward-looking statements caution that clinical outcomes may materially change as patient enrollment continues or more patient data becomes available.”
Read the original on SEC EDGAR ↗
3 Aug 202610-QORIC Pharmaceuticals reported Q2 2026 results with net loss of $41.5 million, R&D expenses increased to $36.3 million, and cash position of $387.6 million; initiated Phase 3 trial for rinzimetostat.earningsopen

Figures in the filing · each found in the filing text

Net loss · H1-2026$-77M
Cash, cash equivalents and investments · Q2-2026$388M
Accumulated deficit · Q2-2026$-770M
Research and development expenses · H1-2026$68M
Operating cash flow · H1-2026$-64M
Free cash flow · H1-2026$-64M

Risks flagged

Clinical trial failure risk

“The successful development of our product candidates is highly uncertain, and we do not believe it is possible at this time to accurately project the nature, timing and estimated costs of the efforts necessary to complete the development of, and obtain regulatory approval for, any of our product candidates.” · word for word

Financing risk

“If events or circumstances occur such that the Company does not obtain additional funding, it will most likely be required to reduce its plans and/or certain discretionary spending, which could have a material adverse effect on the Company’s ability to achieve its intended business objectives.” · word for word

Dependence on key programs

“On August 12, 2025, the Company announced a strategic pipeline prioritization to focus operational and financial resources on the continued advancement of its two lead clinical programs, rinzimetostat and enozertinib. This initiative resulted in a substantial decrease in preclinical research, primarily from the elimination of the Company’s discovery research” · word for word
Read the original on SEC EDGAR ↗
3 Aug 20268-K · 2.02Cash, cash equivalents and investments $388M; R&D expenses $36M (+19% y/y); G&A expenses $9M (+6% y/y)earningsopen

Figures in the filing · each found in the filing text

Cash, cash equivalents and investments · Q2-2026$388M
R&D expenses · Q2-2026$36M+19% y/y
G&A expenses · Q2-2026$9M+6% y/y

Risks flagged

Clinical development risk; Phase 3 trial outcomes uncertain; regulatory approval not guaranteed.

“Initiated Himalayas-1 global Phase 3 registrational trial; primary endpoint radiographic progression-free survival”
Read the original on SEC EDGAR ↗
30 Jul 20268-K · 5.02Reported the departure of a director or principal officer (CEO/CFO change); filed financial statements and exhibits with this reportopen

Risks flagged

Potential dilution from increased share reserve for inducement awards

“Additional 1,100,000 shares reserved for equity awards; total 3,350,000 shares reserved under Inducement Plan.”
Read the original on SEC EDGAR ↗
22 Jun 20268-K · 5.02, 5.07Reported the departure of a director or principal officer (CEO/CFO change); submitted matters to a vote of security holdersopen

Risks flagged

Potential shareholder dilution from increased equity awards; plan amendments approved by stockholders.

“Stockholders approved the A&R 2020 Equity Incentive Plan with 61.2M votes for, 27.3M against.”
Read the original on SEC EDGAR ↗
4 May 202610-QNet loss $-36M (+19% y/y); Research and development expenses $31M (+28% y/y); Cash, cash equivalents and investments $420Mopen

Figures in the filing · each found in the filing text

Net loss · Q1-2026$-36M+19% y/y
Research and development expenses · Q1-2026$31M+28% y/y
Cash, cash equivalents and investments · 2026-03-31$420M
Accumulated deficit · 2026-03-31$-728M

Risks flagged

Clinical trial failure risk

“The successful development of our product candidates is highly uncertain, and we do not believe it is possible at this time to accurately project the nature, timing and estimated costs of the efforts necessary to complete the development of, and obtain regulatory approval for, any of our product candidates.” · word for word

Cash burn and going concern risk

“If events or circumstances occur such that the Company does not obtain additional funding, it will most likely be required to reduce its plans and/or certain discretionary spending, which could have a material adverse effect on the Company’s ability to achieve its intended business objectives.” · word for word
Read the original on SEC EDGAR ↗
4 May 20268-K · 2.02Cash, Cash Equivalents and Investments $420M; R&D Expenses $31M (+28% y/y); G&A Expenses $8M (+1% y/y)earningsopen

Figures in the filing · each found in the filing text

Cash, Cash Equivalents and Investments · Q1-2026$420M
R&D Expenses · Q1-2026$31M+28% y/y
G&A Expenses · Q1-2026$8M+1% y/y
Net Proceeds from ATM · Q1-2026$60M

Risks flagged

Clinical stage company with no revenue; dependent on pipeline success and financing.

“Clinical stage oncology company; no revenue reported; cash burn from R&D.”

R&D expenses increased 27.6% YoY, indicating higher cash burn rate.

“R&D expenses were $31.4 million ... compared to $24.6 million ... an increase of $6.8 million.” · word for word
Read the original on SEC EDGAR ↗
28 Apr 2026DEF 14AProxy statement filed for 2026 annual meeting, seeking stockholder approval to amend the 2020 Equity Incentive Plan with reduced evergreen provision and elimination of repricing authority, and advisory votes on executive compensation.open

Figures in the filing · each found in the filing text

Net Income · FY2025$-129M
Net Income · FY2024$-128M
Burn Rate · FY2023-20254.8%
Overhang · 2026-03-3119.1%
Read the original on SEC EDGAR ↗
31 Mar 20268-K · 8.01ORIC Pharmaceuticals presented dose optimization data from Phase 1b trial of rinzimetostat (ORIC-944); no efficacy or endpoint data disclosed, only dose optimization.SEC ↗
23 Feb 20268-K · 2.02ORIC Pharmaceuticals reports Q4/FY2025 financials: cash $392.3M, R&D $25.9M (Q4), G&A $8.7M (Q4). Clinical updates for rinzimetostat and enozertinib show potential best-in-class data. Cash runway into 2H 2028.earningsopen

Figures in the filing · each found in the filing text

Cash, cash equivalents and investments · FY2025$392M
Research and development expenses · Q4-2025$26M-19% y/y
General and administrative expenses · Q4-2025$9M+14% y/y
Research and development expenses (full year) · FY2025$110M-4% y/y
General and administrative expenses (full year) · FY2025$33M+15% y/y

Risks flagged

Clinical-stage biotech with no approved products; reliance on pipeline success.

“Clinical stage oncology company ... no revenue from product sales disclosed.”
Read the original on SEC EDGAR ↗
23 Feb 202610-KNet loss $-130M; Accumulated deficit $692M; Cash, cash equivalents and investments $392M; Guidance: cash runway into second half of 2028open

Figures in the filing · each found in the filing text

Net loss · FY2025$-130M
Accumulated deficit · 2025-12-31$692M
Cash, cash equivalents and investments · 2025-12-31$392M

Guidance

cash runway into second half of 2028

No revenue guidance; only cash runway guidance provided.

Risks flagged

No approved products or revenue

“We have no products approved for commercial sale and do not anticipate generating any revenue from product sales for the next several years, if ever.” · word for word

Substantial dependence on two product candidates

“We are substantially dependent on the success of our product candidates, rinzimetostat and enozertinib.” · word for word

Clinical trial failure risk

“A failure of one or more clinical trials can occur at any stage of the process.” · word for word
Read the original on SEC EDGAR ↗
23 Feb 20268-K · 8.01Gross proceeds from ATM sales $140Mopen

Figures in the filing · each found in the filing text

Gross proceeds from ATM sales · 2026-02-23$140M

Risks flagged

Dilution risk from ongoing ATM sales

“Company has sold 13.5M shares and may sell up to $200M more, diluting existing shareholders.”
Read the original on SEC EDGAR ↗
8 Dec 20258-K · 8.01Disclosed a material event under other events (litigation, recall, contract loss, or major announcement); filed financial statements and exhibits with this reportopen

Risks flagged

Clinical development risk; early-stage data.

“Phase 1b trial data; no registrational milestones.”
Read the original on SEC EDGAR ↗
13 Nov 20258-K · 7.01Issued a Regulation FD disclosure (forward guidance or material update); filed financial statements and exhibits with this reportopen

Risks flagged

Early-stage clinical data; no regulatory approvals

“Phase 1b trial data; forward-looking statements about potential best-in-class properties”
Read the original on SEC EDGAR ↗
13 Nov 20258-K · 2.02Cash, cash equivalents and investments $413M; R&D expenses $29M (-8% y/y); Net proceeds from ATM program $109Mearningsopen

Figures in the filing · each found in the filing text

Cash, cash equivalents and investments · Q3-2025$413M
R&D expenses · Q3-2025$29M-8% y/y
Net proceeds from ATM program · Q3-2025$109M

Risks flagged

Pre-revenue clinical-stage company; no approved products

“clinical stage oncology company ... no revenue from product sales”

Clinical trial risks for ORIC-944 and enozertinib

“Phase 1b trials; forward-looking statements about potential best-in-class properties”
Read the original on SEC EDGAR ↗
13 Nov 202510-QORIC Pharmaceuticals reported Q3 2025 results with a net loss of $32.6 million, provided positive Phase 1b data for ORIC-944, and announced strategic pipeline prioritization including a 20% workforce reduction.earningsopen

Figures in the filing · each found in the filing text

Net Loss · Q3-2025$-33M-6% y/y
Research and Development Expenses · Q3-2025$29M-8% y/y
Cash, Cash Equivalents and Investments · 2025-09-30$413M
Accumulated Deficit · 2025-09-30$-662M

Risks flagged

Clinical Trial Risk

“The successful development of our product candidates is highly uncertain, and we do not believe it is possible at this time to accurately project the nature, timing and estimated costs of the efforts necessary to complete the development of, and obtain regulatory approval for, any of our product candidates.” · word for word

Financing Risk

“As the Company continues its expansion, it may seek additional financing and/or strategic investments, however, there can be no assurance that any additional financing or strategic investments will be available to the Company on acceptable terms, if at all.” · word for word
Read the original on SEC EDGAR ↗

ORIC Pharmaceuticals, Inc. — questions

What did ORIC Pharmaceuticals, Inc. file recently?
16 SEC filings in the last 12 months. Latest: 8-K on 2026-10-23 — ORIC presented enozertinib (ORIC-114) program update at ESMO 2026, highlighting potential best-in-class profile in 1L EGFR atypical NSCLC, a >$2.5bn market, supporting rapid advancement to Phase 3.

Every figure on this page comes from ORIC Pharmaceuticals, Inc.'s own SEC filings — see them on SEC EDGAR. Price data is licensed and shown only inside the product.

How these figures are read: methodology · EquiReason.