UNITED STATES
                       SECURITIES AND EXCHANGE COMMISSION
                             WASHINGTON, D.C. 20549

                                    FORM 8-K

                                 CURRENT REPORT
                     PURSUANT TO SECTION 13 OR 15(D) OF THE
                         SECURITIES EXCHANGE ACT OF 1934




        Date of Report (Date of earliest event reported): March 23, 2007

                               CELGENE CORPORATION
             (Exact name of registrant as specified in its charter)


           Delaware                       0-16132             22-2711928
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(State or other jurisdiction of   (Commission File Number)   (IRS Employer
        incorporation)                                      Identification No.)



         86 Morris Avenue, Summit, New Jersey                   07901
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       (Address of principal executive offices)               (Zip Code)

       Registrant's telephone number, including area code: (908) 673-9000

             ------------------------------------------------------
         (Former name or former address, if changed since last report.)




Check the appropriate box below if the Form 8-K filing is intended to
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following provisions (see General Instruction A.2. below):

[ ]  Written communications pursuant to Rule 425 under the Securities Act (17
     CFR 230.425)

[ ]  Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17
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[ ]  Pre-commencement communications pursuant to Rule 14d-2(b) under the
     Exchange Act (17 CFR 240.14d-2(b))

[ ]  Pre-commencement communications pursuant to Rule 13e-4(c) under the
     Exchange Act (17 CFR 240.13e-4(c))








ITEM 8.01  OTHER EVENTS


              On March 23, 2007, Celgene Corporation announced that REVLIMID(R)
              (lenalidomide) has received a positive opinion from the European
              Medicines Agency (EMEA) for use in combination with dexamethasone
              as a treatment for patients with multiple myeloma who have
              received at least one prior therapy. The EMEA's Committee for
              Medicinal Products for Human Use (CHMP) has recommended approval
              for REVLIMID(R). The CHMP's positive opinion will be forwarded to
              the European Commission that generally follows the recommendation
              of the CHMP and issues final marketing approval within two to
              three months.

              Attached hereto and incorporated herein by reference as Exhibit
              99.1 is the Press Release announcing such information.


ITEM 9.01   FINANCIAL STATEMENTS AND EXHIBITS.

              (d) Exhibit 99.1 - Press Release dated March 23, 2007







                                   SIGNATURES

Pursuant to the requirements of the Securities and Exchange Act of 1934, the
Registrant has duly caused this report to be signed on its behalf by the
undersigned hereunto duly authorized.


                                             CELGENE CORPORATION



Date:  March 23, 2007                        By: /s/ David W. Gryska
                                                 ----------------------------
                                                 Name:  David W. Gryska
                                                 Title: Sr. Vice President and
                                                        Chief Financial Officer