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Kenneth J. Rollins
+1 858 550 6136
krollins@cooley.com
May 19, 2021
U.S. Securities and Exchange Commission
Division of Corporation Finance
100 F Street, N.E.
Washington, D.C. 20549
Attn: Tracie Mariner, Al Pavot, Deanna Virginio and Irene Paik
Re: | Janux Therapeutics, Inc. |
Draft Registration Statement on Form S-1
Submitted April 16, 2021
CIK No. 0001817713
Ladies and Gentlemen:
On behalf of Janux Therapeutics, Inc. (the “Company”), we are responding to the comments (the “Comments”) of the staff (the “Staff”) of the Securities and Exchange Commission (the “Commission”) contained in its letter, dated May 14, 2021 (the “Comment Letter”), relating to the above referenced confidential Draft Registration Statement on Form S-1 (the “DRS”).
In response to the Comments, the Company has revised the DRS and is publicly filing via EDGAR a revised Registration Statement on Form S-1 (the “Registration Statement”) with this response letter.
For ease of reference, set forth below are the Company’s responses to the Comments. The numbering of the paragraphs below corresponds to the numbering of the Comments, which for your convenience we have incorporated into this response letter. Page references in the text of this response letter correspond to the page numbers of the Registration Statement. Capitalized terms used in this letter but not otherwise defined herein have the meanings set forth in the Registration Statement.
Draft Registration Statement on Form S-1, Submitted April 16, 2021
Prospectus Summary
Overview, page 1
1. | We note your disclosure that “[y]our lead TRACTr product candidates are designed to target PSMA, EGFR, and TROP2,” that your TRACTrs are “designed to be selectively activated in the tumor microenvironment” and that the attachment of the albumin binding domain “is designed to extend the half-life of [y]our TRACTr product candidates.” Please balance these and similar statements relating to the desired or intended purpose of your product candidates with equally prominent explanations that any conclusions regarding desired effects are premature as your product candidates remain in the preclinical or discovery stages and are based on novel technologies. |
Response: In response to the Staff’s comment, the Company has revised its disclosure as requested on pages 1, 2, 16, 86, 100 and 101 of the Registration Statement.
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