CONFIDENTIAL     Page 1 of 3  [*] = Certain confidential information contained in this document, marked by brackets, has  been omitted because it is both (i) not material and (ii) the type that the registrant treats as  private or confidential.  Exhibit 10.6    Seagen Inc.   21823 30th Drive Street   Bothell, WA 98021    March 9, 2023  RemeGen Co., Ltd.  58 Middle Beijing Road  Yantai Economic and Technological Development Zone  Yantai, Shandong Province  China 264006  Attention: CEO  E-mail: [*]    Re: License Agreement dated as of August 8, 2021 and effective as of September 15, 2021  by and between Seagen Inc. (“Seagen”) and RemeGen Co., Ltd. (“RemeGen” and  together with Seagen, collectively, the “Parties” and each a “Party”), as amended by  a Letter Agreement, dated December 7, 2021 (as amended, the “License Agreement”)  Dear [*]:  I refer to recent discussions and alignment at the JCMC between the Parties concerning the  manufacture and supply of RC48 Licensed Product for Development in the Field in the Seagen  Territory.    As contemplated by Section 6.1(a) of the License Agreement, Seagen and RemeGen  entered into that certain Clinical Supply Agreement dated December 15, 2021, as amended by  Amendment No. 1 thereto dated October 11, 2022 (as amended, the “Clinical Supply  Agreement”) for the supply of Bulk Drug Product to Seagen. The purpose of this Letter  Agreement is to memorialize the JCMC decision that Seagen shall be responsible for some of the  clinical manufacture and supply of RC48 Licensed Product for Development in the Field in the  Seagen Territory.   Therefore, Seagen and RemeGen hereby agree as follows:  1. Capitalized terms shall have the meaning ascribed to them in the License Agreement or  Clinical Supply Agreement, as applicable, unless otherwise defined herein.  2. Section 6.1(a) is hereby deleted and replaced in its entirety as follows:   (a) Clinical Supply. RemeGen shall be responsible, by itself or through one or  more Third Party contract manufacturers (each a “CMO”), to manufacture and supply to each  Party, its Affiliates and sublicensees the RC48 Licensed Product for Development in the Field in  the Seagen Territory and in the RemeGen Territory. Within [*] days after the Effective Date, the  Parties shall negotiate in good faith and enter into an agreement consistent with the terms set forth  on Exhibit (a) hereto, pursuant to which RemeGen would supply the RC48 Licensed Product to  
 
 
 Page 2 of 3  [*] = Certain confidential information contained in this document, marked by brackets, has been omitted because it is both (i) not  material and (ii) the type that the registrant treats as private or confidential.  Seagen for use in Development in the Field in the Seagen Territory (or for use in the conduct of  Global Trials or Collaborative Global Trials) at a transfer price [*] (the “RC48 Clinical Supply  Agreement”).  Notwithstanding the foregoing, and without prejudice to the provisions (including  forecasting and ordering procedures) set forth in the RC48 Clinical Supply Agreement, Seagen  may manufacture (or have manufactured) and supply to itself, its Affiliates and sublicensees the  RC48 Licensed Product for use in Development in the Field in the Seagen Territory (and in the  RemeGen Territory for use in the conduct of Global Trials or Collaborative Global Trials).  3. The terms of this Letter Agreement shall be the Confidential Information of both Parties for  purposes of the License Agreement.  4. This Letter Agreement may be amended, or any term hereof modified, only by a written  instrument duly executed by authorized representatives of each of the Parties.    5. This Letter Agreement may be executed in counterparts with the same effect as if both Parties  had signed the same document.  All such counterparts shall be deemed an original, shall be  construed together, and shall constitute one and the same instrument.  Any such counterpart,  to the extent delivered by means of a fax machine or by .pdf, .tif, .gif, .jpeg or similar  attachment to electronic mail (any such delivery, an “Electronic Delivery”) shall be treated  in all manner and respects as an original executed counterpart and shall be considered to have  the same binding legal effect as if it were the original signed version thereof delivered in  person.  No Party hereto shall raise the use of Electronic Delivery to deliver a signature or the  fact that any signature or agreement or instrument was transmitted or communicated through  the use of Electronic Delivery as a defense to the formation of a contract, and each Party  forever waives any such defense, except to the extent that such defense relates to lack of  authenticity.    6. Except as expressly set forth in this Letter Agreement, the terms and conditions of the License  Agreement remain unchanged.  7. This Letter Agreement will be effective as of the date set forth above (the “Effective Date”).    Very truly yours,      [*]   [Signature Page Follows]    
 
 
 Page 3 of 3  [*] = Certain confidential information contained in this document, marked by brackets, has been omitted because it is both (i) not  material and (ii) the type that the registrant treats as private or confidential.  IN WITNESS WHEREOF, the Parties have executed this Letter Agreement as of the Effective  Date by their duly authorized representatives.          SEAGEN INC.      BY:  /s/ Natasha Hernday     NAME:  Natasha Hernday     TITLE: Chief Business Officer          REMEGEN CO., LTD      BY:  /s/ Dan Ross     NAME: Dan Ross      TITLE: Senior Vice President, Global Business Development