Maze Therapeutics, Inc. (MAZE) SEC Filings & Earnings Calls
EquiReason read 14 Maze Therapeutics, Inc. SEC filings in the last 12 months. Latest: 8-K on 2026-10-16 — Maze Therapeutics entered an Exchange Agreement with Frazier Life Sciences; issued pre-funded warrants; dilutive to existing shareholders..
Source: SEC EDGAR filings · figures as of 2026-06-30 · read by EquiReason
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Every filing, read
last 12 months · SECWhat happened, the numbers inside, guidance and risks. The original is one click away.
16 Oct 20268-K · 1.01, 3.02Maze Therapeutics entered an Exchange Agreement with Frazier Life Sciences; issued pre-funded warrants; dilutive to existing shareholders.open
Risks flagged
Dilution risk: Issuance of pre-funded warrants dilutes existing shareholders.
“Item 3.02: issued unregistered shares, diluting existing shareholders.”
Financial distress risk: Exchange agreement may indicate cash constraints.
“Entry into Exchange Agreement with Frazier Life Sciences.”
11 Aug 20268-K · 2.02Cash, cash equivalents and marketable securities $495M; License revenue $20M; Research & Development expenses $35M (+24% y/y); Guidance: Cash runway into 2029earningsopen
Figures in the filing · each found in the filing text
| Cash, cash equivalents and marketable securities · Q2-2026 | $495M | |
| License revenue · H1-2026 | $20M | |
| Research & Development expenses · Q2-2026 | $35M | +24% y/y |
| Research & Development expenses · H1-2026 | $69M | +24% y/y |
| General & Administrative expenses · Q2-2026 | $13M | +56% y/y |
| General & Administrative expenses · H1-2026 | $26M | +57% y/y |
| Net loss · Q2-2026 | $-45M | +33% y/y |
| Net loss per share · Q2-2026 | $-0.76 | -1% y/y |
Guidance
Cash runway into 2029
Management reaffirms cash runway into 2029 and clinical milestones, no revenue guidance.
Risks flagged
Clinical-stage company with no approved products, relies on pipeline success.
“No license revenue in Q2 2026; net loss widening.”
Increased operating expenses may pressure cash runway if milestones are delayed.
“R&D and G&A expenses increased significantly YoY.”
11 Aug 202610-QQ2 2026 results: first license revenue of $20M recognized, net loss increased to $68.9M, cash position strengthened to $494.9M.earningsopen
Figures in the filing · each found in the filing text
| License revenue · H1-2026 | $20M | |
| Net loss · H1-2026 | $-69M | |
| Cash and cash equivalents · 2026-06-30 | $203M | |
| Research and development expense · H1-2026 | $69M | +24% y/y |
| General and administrative expense · H1-2026 | $26M | +58% y/y |
| Operating cash flow · H1-2026 | $-54M |
Risks flagged
Clinical-stage biopharmaceutical company with no product revenue and significant losses
“We are a clinical-stage biopharmaceutical company with a limited operating history... Since our inception, we have incurred significant operating losses and have not generated any product revenue.” · word for word
Dependence on successful development and commercialization of lead programs
“We are early in our development efforts and highly dependent on the success of our lead programs.” · word for word
Need for substantial additional capital
“We will require substantial additional capital to finance our operations and achieve our goals.” · word for word
22 May 20268-K · 5.02Reported a director or officer change (departure, election, appointment or pay arrangement)open
Risks flagged
Key finance executive departure; transition risk minimal as CFO assumes duties.
“resignation was not as a result of any disagreement”
12 May 20268-K · 2.02Net loss $-24M; Cash, cash equivalents and marketable securities $363M; License revenue $20Mearningsopen
Figures in the filing · each found in the filing text
| Net loss · Q1-2026 | $-24M | |
| Cash, cash equivalents and marketable securities · Q1-2026 | $363M | |
| License revenue · Q1-2026 | $20M | |
| R&D expenses · Q1-2026 | $34M | |
| G&A expenses · Q1-2026 | $12M | |
| Net loss per share · Q1-2026 | $-0.45 |
Risks flagged
Clinical trial risk: MZE829 and MZE782 are in Phase 2; failure in pivotal trials could impair value.
“Maze plans to initiate a pivotal trial in patients with moderate AMKD without diabetes, including those with FSGS, in the first half of 2027, subject to regulatory feedback.” · word for word
Regulatory risk: FDA feedback required for pivotal trial design; delays possible.
“Subject to regulatory feedback.” · word for word
12 May 202610-QLicense revenue $20M; Research and development expenses $34M (+24% y/y); General and administrative expenses $12M (+59% y/y)open
Figures in the filing · each found in the filing text
| License revenue · Q1-2026 | $20M | |
| Research and development expenses · Q1-2026 | $34M | +24% y/y |
| General and administrative expenses · Q1-2026 | $12M | +59% y/y |
| Net loss · Q1-2026 | $-24M | -26% y/y |
| Cash, cash equivalents and marketable securities · 2026-03-31 | $363M | |
| Accumulated deficit · 2026-03-31 | $514M | |
| Net cash used in operating activities · Q1-2026 | $-39M | +33% y/y |
| Stock-based compensation expense · Q1-2026 | $7M | +120% y/y |
| Interest and other income, net · Q1-2026 | $3M | +23% y/y |
| Interest expense · Q1-2026 | $866000.00 |
Risks flagged
Significant operating losses and negative cash flows
“The Company has incurred significant losses and negative cash flows from operations and expects to incur significant and increasing losses as a result of its continued research and development activities.” · word for word
Dependence on future financing
“The Company may seek to raise capital through additional term loan tranches pursuant to the Hercules Term Loan Facility, equity financings, including pursuant to the 2026 Sale Agreement, license agreements, or other sources of financing. There can be no assurance that such financing will be available or will be at terms acceptable to the Company.” · word for word
Early-stage pipeline with no approved products
“We are a clinical-stage biopharmaceutical company with a limited operating history, which may make it difficult to evaluate the success of our business to date and to assess our future viability. Since our inception, we have incurred significant operating losses and have not generated any product revenue.” · word for word
Reliance on collaborations for revenue
“We have entered, and may in the future enter, into strategic collaborations, transactions and licensing partnerships for research, development or commercialization of our programs, including our first therapeutic candidate MZE001, and we may not be able to realize the full value of these partnerships or our partnered programs.” · word for word
22 Apr 20268-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
Dilution risk; use of proceeds for early-stage pipeline may not yield returns.
“use any net proceeds ... to advance research and development of the Company’s product candidates”
25 Mar 202610-KNet loss $-131M; Net income $52M; Cash, cash equivalents, and marketable securities $360Mopen
Figures in the filing · each found in the filing text
| Net loss · FY2025 | $-131M | |
| Net income · FY2024 | $52M | |
| Cash, cash equivalents, and marketable securities · 2025-12-31 | $360M | |
| Accumulated deficit · 2025-12-31 | $-490M |
Risks flagged
No product revenue and significant losses
“Since our inception, we have incurred significant operating losses and have not generated any product revenue.” · word for word
Need for additional capital
“We will require substantial additional capital to finance our operations and achieve our goals.” · word for word
Clinical trial and regulatory risk
“Our lead programs are still in early clinical development, and we are subject to the risks of failure inherent in the development of therapeutic candidates based on novel technologies.” · word for word
Reliance on third-party manufacturers and CROs
“We rely on third parties to conduct current and future clinical trials, and those third parties may not perform satisfactorily or at all.” · word for word
Supply chain and geopolitical risk (BIOSECURE Act)
“We are currently parties to agreements with WuXi... If these bills become law... we may be restricted in our ability to work with WuXi and other Chinese biotechnology manufacturing companies.” · word for word
25 Mar 20268-K · 2.02, 5.02, 7.01Cash, cash equivalents and marketable securities $360M; Mean reduction in uACR (broad AMKD) 35.6; Mean reduction in uACR (severe FSGS) 61.8; Guidance: Cash runway into 2028earningsopen
Figures in the filing · each found in the filing text
| Cash, cash equivalents and marketable securities · FY2025 | $360M | |
| Mean reduction in uACR (broad AMKD) · AMKD · week_12 | 35.6% | |
| Mean reduction in uACR (severe FSGS) · FSGS · week_12 | 61.8% | |
| Mean reduction in uACR (AMKD without diabetes) · AMKD without diabetes · week_12 | 48.6% |
Guidance
Cash runway into 2028
Management reaffirms cash runway and pipeline milestones; positive tone on clinical data.
Risks flagged
Clinical-stage company with no approved products; data still early stage.
“Phase 2 data, not yet pivotal; regulatory feedback needed.”
4 Feb 20268-K · 1.01, 1.02, 2.03Maze Therapeutics terminated its existing loan with Banc of California and entered into a new loan agreement with Hercules Capital, creating a direct financial obligation.open
Risks flagged
New debt obligation may increase financial leverage; terms not disclosed.
“Creation of a direct financial obligation; termination of prior loan.”
6 Nov 202510-QMaze Therapeutics reported Q3 2025 results: net loss of $30.1M, no license revenue, cash position of $383.9M after private placement.earningsopen
Figures in the filing · each found in the filing text
| Cash and cash equivalents · Q3-2025 | $317M | |
| Marketable securities · Q3-2025 | $67M | |
| Net loss · Q3-2025 | $-30M | |
| Research and development expense · Q3-2025 | $25M | |
| General and administrative expense · Q3-2025 | $8M | |
| Accumulated deficit · Q3-2025 | $455M | |
| Interest and other income, net · Q3-2025 | $3M | |
| Operating cash flow · 9M-2025 | $-84M |
Risks flagged
No product revenue, pre-commercial stage
“Since our inception, we have incurred significant operating losses and have not generated any product revenue.” · word for word
Dependence on clinical trial success
“We are early in our development efforts and highly dependent on the success of our lead programs.” · word for word
Need for additional capital
“We will require substantial additional capital to finance our operations and achieve our goals.” · word for word
6 Nov 20258-K · 2.02Cash, cash equivalents and marketable securities $384M; Net loss $-30M; R&D expenses $25M; Guidance: Cash runway into 2028earningsopen
Figures in the filing · each found in the filing text
| Cash, cash equivalents and marketable securities · Q3-2025 | $384M | |
| Net loss · Q3-2025 | $-30M | |
| R&D expenses · Q3-2025 | $25M | |
| G&A expenses · Q3-2025 | $8M |
Guidance
Cash runway into 2028
Management expressed positive outlook with strong cash position and pipeline milestones.
Risks flagged
No revenue from license agreements; reliance on pipeline success.
“No license revenue was recognized during the three and nine months ended September 30, 2025.” · word for word
Maze Therapeutics, Inc. — questions
- What did Maze Therapeutics, Inc. file recently?
- 14 SEC filings in the last 12 months. Latest: 8-K on 2026-10-16 — Maze Therapeutics entered an Exchange Agreement with Frazier Life Sciences; issued pre-funded warrants; dilutive to existing shareholders.
Every figure on this page comes from Maze 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.