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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

KYMRKymera Therapeutics, Inc.Follow KYMR — free
Biotechnology · Healthcare
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Market cap
9.2B
P/E TTM
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52-week
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Next earnings
29 Oct, in 5 days

Every filing, read

last 12 months · SEC

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

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
Read the original on SEC EDGAR ↗
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.”
Read the original on SEC EDGAR ↗
27 Jul 20268-K · 5.02, 7.01Reported the departure of a director or principal officer (CEO/CFO change); issued a Regulation FD disclosure (forward guidance or material update)SEC ↗
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 · 2026-06-261,630,658

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
Read the original on SEC EDGAR ↗
26 Jun 2026SC 13D/ASchedule 13D/A: BIOTECHNOLOGY VALUE FUND L P 6.3%SEC ↗
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.”
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
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 · FY202588.0%
CEO at-risk pay percentage · FY202592.0%

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
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
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.”
Read the original on SEC EDGAR ↗
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.”
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
15 Dec 2025SC 13D/ASchedule 13D/A: BIOTECHNOLOGY VALUE FUND L P 8.5%SEC ↗
11 Dec 2025SC 13D/ASchedule 13D/A: Baker Bros. Advisors LP 10.9%SEC ↗
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”
Read the original on SEC EDGAR ↗
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) · Q4-202598.0%
EASI reduction · Q4-202563.0%
Peak pruritus NRS reduction · Q4-202540.0%
Read the original on SEC EDGAR ↗
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) · Q4-202598.0%
EASI reduction · Q4-202563.0%
Peak pruritus NRS reduction · Q4-202540.0%
Read the original on SEC EDGAR ↗
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”
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗

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.