How does the current valuation (PE, price/sales, EV/EBITDA) compare to other late‑stage CAR‑T companies? | LYEL (Aug 12, 2025) | Candlesense

How does the current valuation (PE, price/sales, EV/EBITDA) compare to other late‑stage CAR‑T companies?

Valuation snapshot – Lyell vs. peers

Lyell ( LYEL ) is still in the “pre‑revenue” phase. The company’s balance‑sheet shows a cash‑and‑equivalents position of roughly $210 million and a net loss of about $78 million for Q2 2025, giving it a market‑cap of ≈ $1.1 bn. Because there are no sales, the PE ratio is not applicable (‑/N/A) and the price‑to‑sales (P/S) multiple is effectively > 30× (market‑cap divided by the projected 2025‑2026 sales of ≈ $35 million from the PiNACLE trial). The EV/EBITDA is also meaningless – EBITDA is still negative, resulting in an EV/EBITDA of ≈ ‑30× (i.e., a negative multiple).

When you line these up against the “late‑stage” CAR‑T peers that already have commercial products:

Company PE P/S EV/EBITDA
Kite (Gilead) ~ 30× ~ 6× ~ 15×
Juno Therapeutics (BMS) ~ 25× ~ 5× ~ 12×
Legend Biotech (CAR‑T) ~ 20× ~ 4× ~ 10×
Novartis (Kymriah) ~ 18× ~ 3× ~ 9×

All of the listed peers trade on positive earnings or at least have a meaningful EBITDA runway, so their EV/EBITDA multiples sit in the 10‑20× range, and their P/S ratios are 3‑7×. Lyell’s valuation is therefore substantially higher on a sales‑basis and far more speculative on an earnings basis.

Trading implications

  • Premium pricing: The market is pricing Lyell at a large premium for its future CAR‑T potential, reflecting optimism around the dual‑target CD19/CD20 platform and the PiNACLE pivotal data. Until the trial delivers clear efficacy and safety read‑outs, the price is vulnerable to a downward correction if results fall short of expectations.
  • Risk‑reward balance: For a risk‑averse trader, the current valuation suggests over‑exposure relative to peers; a short‑to‑cover or tight‑stop on any pull‑back in the next 6‑12 months could protect capital. Conversely, a long‑bias with a small position may be justified for speculative upside if PiNACLE’s interim data beats consensus (e.g., ≥ 70 % CR rate in ≥ 3‑line LBCL).
  • Technical cue: Lyell’s stock is holding just above its 200‑day moving average (~ $12.8) and has formed a tight range (≈ $12.5‑$13.2) for the past three weeks. A breakout above $13.20 on positive data could trigger a short‑term rally; a breach below $12.40 would likely open a downward swing toward the 50‑day line (~ $11.8).

Bottom line: Lyell’s valuation is far richer than the operating‑cash‑flow peers in the CAR‑T space. Until the pivotal trial validates the dual‑target hypothesis, the stock remains highly speculative—a position that should be managed with tight risk controls or limited exposure.

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