Kymera Therapeutics, Inc. (KYMR) SEC Filings & Earnings Calls
EquiReason read 21 Kymera Therapeutics, Inc. SEC filings in the last 12 months. Latest: 10-Q on 2026-08-05 — Kymera Therapeutics reported Q2 2026 results with collaboration revenue of $65M driven by Gilead option exercise and Sanofi milestone, net loss improved to $61.2M from $76.6M year-.
Source: SEC EDGAR filings · figures as of 2026-06-30 · read by EquiReason
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5 Aug 202610-QKymera Therapeutics reported Q2 2026 results with collaboration revenue of $65M driven by Gilead option exercise and Sanofi milestone, net loss improved to $61.2M from $76.6M year-over-year.earningsopen
Figures in the filing · each found in the filing text
| Collaboration revenue · Q2-2026 | $65M | +466% y/y |
| Net loss · Q2-2026 | $-61M | -20% y/y |
| Research and development expense · Q2-2026 | $119M | +52% y/y |
| General and administrative expense · Q2-2026 | $21M | +20% y/y |
| Cash, cash equivalents and marketable securities · 2026-06-30 | $1.50B | |
| Accumulated deficit · 2026-06-30 | $-1.20B |
Risks flagged
Clinical-stage biotech risk
“We are a clinical stage company and that may make it difficult for our stockholders to evaluate the success of our business to date and to assess our future viability.” · word for word
Continued operating losses
“We have incurred significant operating losses since our inception and anticipate that we will incur continued losses for the foreseeable future.” · word for word
Need for additional funding
“We will need to raise substantial additional funding. If we are unable to raise capital when needed or on attractive terms, we would be forced to delay, scale back or discontinue some of our product candidate development programs or future commercialization efforts.” · word for word
5 Aug 20268-K · 2.02Cash and cash equivalents $1.50Bearningsopen
Figures in the filing · each found in the filing text
| Cash and cash equivalents · Q2-2026 | $1.50B |
Risks flagged
Clinical-stage biopharma; no approved products; reliance on pipeline success.
“Company is clinical-stage; no approved products; pipeline risk.”
26 Jun 2026SC 13D/ABVF group sold 1,630,658 shares of Kymera Therapeutics, reducing their aggregate beneficial ownership to 6.3%.open
Figures in the filing · each found in the filing text
| Shares sold by BVF group · 2026-06-26 | 1,630,658 |
Risks flagged
Activist/insider selling pressure
“On June 26, 2026, the Reporting Persons and the Partners Managed Account sold an aggregate of 1,630,658 Shares at a price per Share of $106.50.” · word for word
25 Jun 20268-K · 7.01, 8.01Issued a Regulation FD disclosure (forward guidance or material update); disclosed a material event under other events (litigation, recall, contract loss, or major announcement)open
Risks flagged
Clinical trial risks remain; forward-looking statements caution about uncertainties.
“uncertainties inherent in the initiation, timing and design of ongoing and future clinical trials, the availability and timing of data... ability to successfully demonstrate the safety and efficacy of drug candidates.”
8 Jun 20268-K · 5.02Reported a director or officer change (departure, election, appointment or pay arrangement)open
Risks flagged
Loss of COO could impact operational execution, but transition to advisor role mitigates risk.
“Mr. Chadwick will remain an employee of Kymera Therapeutics, Inc. as an advisor until November 2026.” · word for word
30 Apr 20268-K · 2.02Cash and cash equivalents $1.55Bearningsopen
Figures in the filing · each found in the filing text
| Cash and cash equivalents · Q1-2026 | $1.55B |
Risks flagged
Clinical trial execution risk for KT-621 and KT-579.
“Data expected by mid-2027 and late 2027 for KT-621; KT-579 data in 2H26.” · word for word
30 Apr 202610-QKymera reported Q1 2026 results: collaboration revenue increased to $34.4M, net loss widened to $69.2M, and cash position remains strong at $1.546B.earningsopen
Figures in the filing · each found in the filing text
| Collaboration revenue · Q1-2026 | $34M | +56% y/y |
| Net loss · Q1-2026 | $-69M | +6% y/y |
| Research and development expenses · Q1-2026 | $98M | +22% y/y |
| Cash, cash equivalents and marketable securities · 2026-03-31 | $1.55B | |
| Accumulated deficit · 2026-03-31 | $1.14B |
Risks flagged
Clinical-stage company with no approved products
“We are a clinical stage company and that may make it difficult for our stockholders to evaluate the success of our business to date and to assess our future viability.” · word for word
Continued operating losses and need for additional funding
“We have incurred significant operating losses since our inception and anticipate that we will incur continued losses for the foreseeable future.” · word for word
Dependence on collaboration partners (Sanofi, Gilead)
“If we are unable to advance them through the clinic for safety or efficacy reasons or commercialize our product candidates or experience significant delays in doing so, our business will be materially harmed.” · word for word
29 Apr 2026DEF 14AAnnual proxy statement filed for 2026 shareholder meeting, detailing executive compensation, governance, and shareholder proposals.open
Figures in the filing · each found in the filing text
| Cash, cash equivalents and marketable securities · FY2025 | $1.60B | |
| Gross proceeds from follow-on equity offerings · FY2025 | $981M | |
| Sanofi milestone payment · FY2025 | $20M | |
| Gilead upfront payment · FY2025 | $40M | |
| CEO total compensation · FY2025 | $9M | |
| Net loss · FY2025 | $-311M | |
| Total Shareholder Return (TSR) · FY2025 | $125.50 | |
| CEO pay ratio · FY2025 | $21.00 | |
| Say-on-Pay support percentage · FY2025 | 88.0% | |
| CEO at-risk pay percentage · FY2025 | 92.0% |
Risks flagged
Clinical-stage biotech with no approved products
“We are a clinical-stage biopharmaceutical company dedicated to reinventing the treatment of human disease through the development of innovative, highly differentiated oral medicines.” · word for word
Significant net losses and accumulated deficit
“Net Loss ($ thousands) 311,351”
Dependence on key clinical trial outcomes
“The shares vest upon achievement of certain milestones related to KT-621 clinical development and clinical development of our other programs.” · word for word
Potential dilution from equity compensation
“The 2020 Plan provides that the number of shares reserved and available for issuance under the plan will automatically increase each January 1, beginning on January 1, 2021, by 4% of the outstanding number of shares of common stock.” · word for word
Concentration of ownership by large institutional holders
“Entities affiliated with Baker Bros. Advisors LP 8,680,353 10.56%” · word for word
26 Feb 202610-KNet Income (Loss) $-267M; Research and Development Expense $267Mopen
Figures in the filing · each found in the filing text
| Net Income (Loss) · FY2025 | $-267M | |
| Research and Development Expense · FY2025 | $267M |
Risks flagged
Clinical Development Risk
“We are very early in our development efforts and our product candidates, whether conducted by us or our collaborators, are in early clinical development.” · word for word
Funding Risk
“We will need to raise substantial additional funding. If we are unable to raise capital when needed or on attractive terms, we would be forced to delay, scale back or discontinue some of our product candidate development programs.” · word for word
Novel Technology Risk
“Our approach to the discovery and development of product candidates is novel and unproven, which makes it difficult to predict the time, cost of development and likelihood of successfully developing any products.” · word for word
26 Feb 20268-K · 1.01, 1.02, 8.01Entered $500M at-the-market offering program; terminated prior ATM with Jefferies; also filed resale prospectus for selling stockholders up to 31.4M shares.open
Risks flagged
Dilution risk from ATM and resale registration
“Up to $500M ATM offering and registration of 31.4M shares for selling stockholders.”
26 Feb 20268-K · 2.02Cash and cash equivalents $1.60Bearningsopen
Figures in the filing · each found in the filing text
| Cash and cash equivalents · Q4-2025 | $1.60B |
Risks flagged
Clinical trial execution risk for KT-621 and KT-579
“Phase 2b trials for KT-621 ongoing; Phase 1 for KT-579 initiated; data expected in 2027 and 2H26.”
13 Jan 20268-K · 2.02, 7.01Cash, cash equivalents and marketable securities $1.60Bearningsopen
Figures in the filing · each found in the filing text
| Cash, cash equivalents and marketable securities · Q4-2025 | $1.60B |
Risks flagged
Clinical trial risk; pipeline programs still in Phase 2.
“KT-621 BROADEN2 Phase 2b trial in AD ongoing, with data expected by mid-2027” · word for word
10 Dec 20258-K · 1.01, 8.01Net proceeds from offering $656Mopen
Figures in the filing · each found in the filing text
| Net proceeds from offering · Q4-2025 | $656M |
Risks flagged
Dilution risk from equity offering
“Issuance of 8,050,000 shares at $86.00 per share”
8 Dec 20258-K · 7.01, 8.01STAT6 degradation (blood) 98; EASI reduction 63; Peak pruritus NRS reduction 40open
Figures in the filing · each found in the filing text
| STAT6 degradation (blood) · Q4-2025 | 98.0% | |
| EASI reduction · Q4-2025 | 63.0% | |
| Peak pruritus NRS reduction · Q4-2025 | 40.0% |
8 Dec 20258-K · 7.01STAT6 degradation (blood) 98; EASI reduction 63; Peak pruritus NRS reduction 40open
Figures in the filing · each found in the filing text
| STAT6 degradation (blood) · Q4-2025 | 98.0% | |
| EASI reduction · Q4-2025 | 63.0% | |
| Peak pruritus NRS reduction · Q4-2025 | 40.0% |
4 Nov 20258-K · 2.02Cash and cash equivalents $979Mearningsopen
Figures in the filing · each found in the filing text
| Cash and cash equivalents · Q3-2025 | $979M |
Risks flagged
Pre-revenue clinical-stage company with no approved products; reliance on pipeline success
“No revenue from product sales; net loss expected; cash burn for R&D”
4 Nov 202510-QKymera reported Q3 2025 results: net loss widened to $82.2M on higher R&D spend; cash position strong at $978.7M; new Gilead collaboration and Sanofi milestone highlight partner interest.earningsopen
Figures in the filing · each found in the filing text
| Cash, cash equivalents and marketable securities · Q3-2025 | $979M | |
| Collaboration revenue · Q3-2025 | $3M | -26% y/y |
| Net loss · Q3-2025 | $-82M | +32% y/y |
| Research and development expenses · Q3-2025 | $74M | +23% y/y |
| Accumulated deficit · Q3-2025 | $-979M | |
| Cash used in operating activities · 9M-2025 | $-166M | +25% y/y |
| Free cash flow · 9M-2025 | $-167M |
Risks flagged
Clinical-stage company with no approved products
“We are a clinical stage company and that may make it difficult for our stockholders to evaluate the success of our business to date and to assess our future viability.” · word for word
Continued operating losses and need for additional funding
“We have incurred significant operating losses since our inception and anticipate that we will incur continued losses for the foreseeable future.” · word for word
Novel and unproven technology platform
“Our approach to the discovery and development of product candidates is novel and unproven, which makes it difficult to predict the time, cost of development and likelihood of successfully developing any products.” · word for word
Dependence on third-party manufacturers and CROs
“We rely, and expect to continue to rely, on third parties to conduct our ongoing and planned preclinical studies and clinical trials for our current and future product candidates.” · word for word
Sublease market risk for vacated lab space
“The Company will continue to evaluate the potential recovery of the asset group under sublease scenarios, and thus it is possible that further additional impairments could be identified in future periods, and such amounts could be material.” · word for word
Kymera Therapeutics, Inc. — questions
- What did Kymera Therapeutics, Inc. file recently?
- 21 SEC filings in the last 12 months. Latest: 10-Q on 2026-08-05 — Kymera Therapeutics reported Q2 2026 results with collaboration revenue of $65M driven by Gilead option exercise and Sanofi milestone, net loss improved to $61.2M from $76.6M year-over-year.
Every figure on this page comes from Kymera Therapeutics, 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.