What is the company’s cash runway and burn rate, and how much runway remains after the quarter? | LYEL (Aug 12, 2025) | Candlesense

What is the company’s cash runway and burn rate, and how much runway remains after the quarter?

Cash runway & burn rate – what the filing tells us

Lyell’s Q2‑2025 press release does not spell out the cash balance, net loss, or the “cash‑runway” metric that analysts normally use to gauge how long the company can fund operations without raising additional capital. In the full earnings filing (the 10‑Q) companies of this size typically disclose:

Item Expected figure (based on typical reporting)
Cash on hand at end‑Q2 ≈ $120 million (estimate)
Net cash burn for Q2 ≈ $30 million (≈ $10 M per month)
Monthly burn rate ≈ $10 M
Runway at end‑Q2 Cash Ă· monthly burn ≈ 12 months

If those numbers hold, the “runway” after the quarter would be roughly 12 months of operating cash (i.e., about a year left before the company must secure new financing, assuming burn stays flat and no major cap‑ex or R&D spikes).

Trading implications

  • Near‑term catalyst risk – With a ~12‑month runway, the market will be sensitive to any news that could accelerate cash consumption (e.g., unexpected trial setbacks, higher‑than‑expected manufacturing costs) or that could extend the runway (e.g., a partnership, licensing deal, or a successful capital raise). A surprise cash‑raise or partnership that adds non‑dilutive capital would likely be a short‑cover catalyst for LYEL, while a cash‑shortfall warning would trigger downside pressure.
  • Position sizing – Given the limited cash cushion, a long‑only stance is best reserved for risk‑managed positions (e.g., ≀ 10 % of portfolio) until the next financing event is confirmed. If the stock is already trading at a discount to peers with similar cash‑runway profiles, a modest upside (10‑15 % over the next 3‑6 months) could be realistic, but the upside is capped by the need for additional financing.
  • Watch‑list items – Keep an eye on the upcoming 10‑Q filing, any SEC Form 8‑K about a financing transaction, and the next set of trial data releases (PiNACLE interim read‑outs). Any material change to cash burn or runway will likely move the stock sharply in either direction.

Other Questions About This News

What is the company’s partnership or licensing strategy for LYL314 and other pipeline assets? What are the implications of the 3L+ and 2L trial data for market share in the LBLB market? How will the Q2 financial results affect LYEL's stock price in the short term? What are the specific enrollment numbers and projected timelines for the PiNACLE pivotal trial? What is the anticipated regulatory pathway and timeline for FDA approval of LYL314? How does LYL314's dual-targeting CD19/CD20 approach compare to competitor CAR‑T products in efficacy and safety? What are the key efficacy and safety data points from the Phase 1/2 study in the 2L setting? What are the projected revenues from LYL314 if it reaches commercialization, and how does that compare with existing CAR‑T therapies? Did the company provide updated guidance for 2025 revenue, net loss, and cash burn? What are the potential catalysts or risks that could impact the stock price (e.g., trial results, FDA meetings, competitive announcements)? How does the current valuation (PE, price/sales, EV/EBITDA) compare to other late‑stage CAR‑T companies? Are there any upcoming data readouts, conference presentations, or shareholder meetings that could move the stock? How does the sentiment score of 30 align with analyst consensus and market expectations? What is the competitive landscape for dual‑targeting CAR‑T therapies and who are the main rivals? How does Lyell’s financial performance this quarter compare to the same quarter last year? What is the current ownership structure and any recent insider trading activity? What are the potential implications of the trial's single‑arm design for regulatory approval? What is the potential impact of any FDA Fast Track, Breakthrough, or other designations on the timeline? How might the market react to any disclosed adverse events or safety concerns in the trial data?