Updated 23 Oct 2026, 16:35 CEST. First published 23 Oct 2026, 16:19 CEST. This page is revised in place as the story develops.
Lycia Therapeutics, a South San Francisco company developing drugs designed to degrade disease-causing proteins outside cells, was expected to begin trading on the Nasdaq Global Select Market as LYCA on 23 October 2026 after pricing a larger offering than it first planned. Its preliminary prospectus, dated 20 October 2026, offered 14,700,000 shares at $16.00 to $18.00 each. On 22 October 2026 it priced 17,640,000 shares at $18.00, the top of that range, for expected gross proceeds of about $317.5m before underwriting discounts and other expenses. All shares in the offering will be sold by the company.
- IPO price · 22 October 202618.00 $ per share
- Shares priced · 22 October 202617,640,000 shares
- Expected gross proceeds · 22 October 2026317.5 $m
- Preliminary price range · 20 October 202616.00-18.00 $ per share
- Underwriters' option · 22 October 20262,646,000 shares
- Trading: expected to begin on 23 October 2026 on the Nasdaq Global Select Market, ticker LYCA
- Closing: expected on 26 October 2026, subject to customary closing conditions
- Joint book-running managers: Jefferies, TD Cowen, Evercore ISI and Guggenheim Securities; LifeSci Capital is passive book-running manager
- Underwriters have a 30-day option to buy up to 2,646,000 more shares at the IPO price, less underwriting discounts and commissions
What Lycia develops
Lycia is a clinical-stage company with an initial focus on autoimmune, inflammatory and allergic diseases. Its LYTAC (Lysosomal Targeting Chimera) platform builds on work by Nobel laureate Carolyn Bertozzi, Ph.D., professor of chemistry and HHMI investigator at Stanford University. According to its prospectus, existing degrader approaches such as PROTACs and molecular glues are generally limited to proteins inside cells. Its lead candidates are LCA-0061, a degrader of IgE for food allergy and other allergic diseases, and LCA-0321, designed to degrade the autoantibodies that the company describes as the drivers of Graves' disease. A second IgE degrader, LCA-0062, which the prospectus calls a fast-follower program, is in Investigational New Drug (IND)-enabling activities.
LCA-0061, LCA-0062 and LCA-0321 are investigational therapeutic candidates, and none has been approved: the prospectus says Lycia has not completed any clinical trials and has no products approved for commercial sale. Among the risk factors it lists, Lycia says it has incurred significant operating losses since its inception and has not generated any revenue from product sales. It reported a net loss of $36.5m for 2025 and $19.2m for the six months to 30 June 2026, and an accumulated deficit of $136.8m at 30 June 2026.
- Lycia Therapeutics, Announces Pricing of Upsized Initial Public Offering (GlobeNewswire), 23 Oct 2026, 01:51 CEST
- Lycia Therapeutics, Form S-1/A preliminary prospectus (SEC EDGAR), 20 Oct 2026, 12:09 CEST