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These products may not be approved and/or licensed in all countries where this website is accessible. For information about Celgene products and services in countries other than the U.S., please contact the local office (as listed under the Global Network). [PRODUCT MONOGRAPH TEMPLATE Page 1of 92 PRODUCT MONOGRAPH Pr REVLIMID® lenalidomidecapsules 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg and 25 mg Antineoplastic Agent Immunomodulatory Agent Celgene Inc. REMOTE SUPPORT PORTALSupport Portal
CELGENE REPORTS FOURTH QUARTER AND FULL YEAR 2018 - Exceeded 2018 top- and bottom-line guidance - 2019 guidance reflects strong operating momentum leading to double-digit top- and bottom-line growth; Reaffirming 2020 financial outlook - Advancing five late-stage assets with U.S. approvals expected through 2020; Ozanimod U.S. and EU regulatory submissions on-track for Q1:2019 Celgene Corporation (NASDAQ: CELG) reported operating results for OTEZLA-15JUL2019-VER2.3.01 Otexla Safety Data Sheet. Otezla-15Jul2019-Ver2.3.01 REVLIMID (LENALIDOMIDE) RELAPSED/REFRACTORY OTEZLA® (apremilast) Psoriatic arthritis CC-90001 Fibrosis CC-220 Systemic lupus erythematosus Psoriasis (Japan) Ankylosing spondylitis Behçet’s disease Atopic dermatitis Ulcerative colitis Psoriasis Crohn's disease ozanimod Relapsing multiple sclerosis Ulcerativecolitis
[PRODUCT MONOGRAPH TEMPLATE Page 5of 50 WARNINGS AND PRECAUTIONS General Albumin (Human): ABRAXANE® for Injectable Suspension (paclitaxel powder for injectable suspension) (nanoparticle, albumin-bound paclitaxel) contains albumin (human), a derivative of human blood and is a 抗造血器悪性腫瘍剤ポマリスト ボルテゾミブ及びデキサメタゾン … 1 2019 年5 月22 日 報道関係各位 セルジーン株式会社 抗造血器悪性腫瘍剤ポマリスト ®、 ボルテゾミブ及びデキサメタゾンとの3 剤併用療法追加による CELGENE GLOBAL OFFICE LOCATIONS With locations around the world, Celgene is impacting the lives of patients with cancer, inflammatory diseases, and other serious illnesses around the world. Find here the contact information and website access to our global office locations. CELGENE CORPORATION TO ACQUIRE JUNO THERAPEUTICS, INC SUMMIT, N.J. & SEATTLE– (BUSINESS WIRE)– Celgene Corporation (NASDAQ:CELG) and Juno Therapeutics, Inc. (NASDAQ:JUNO) today announced the signing of a definitive merger agreement in which Celgene has agreed to acquire Juno. Under the terms of the merger agreement, Celgene will pay $87 per share in cash, or a total of approximately $9 billionVIDAZA® LOGO
These products may not be approved and/or licensed in all countries where this website is accessible. For information about Celgene products and services in countries other than the U.S., please contact the local office (as listed under the Global Network). [PRODUCT MONOGRAPH TEMPLATE Page 1of 92 PRODUCT MONOGRAPH Pr REVLIMID® lenalidomidecapsules 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg and 25 mg Antineoplastic Agent Immunomodulatory Agent Celgene Inc. REMOTE SUPPORT PORTALSupport Portal
CELGENE REPORTS FOURTH QUARTER AND FULL YEAR 2018 - Exceeded 2018 top- and bottom-line guidance - 2019 guidance reflects strong operating momentum leading to double-digit top- and bottom-line growth; Reaffirming 2020 financial outlook - Advancing five late-stage assets with U.S. approvals expected through 2020; Ozanimod U.S. and EU regulatory submissions on-track for Q1:2019 Celgene Corporation (NASDAQ: CELG) reported operating results for OTEZLA-15JUL2019-VER2.3.01 Otexla Safety Data Sheet. Otezla-15Jul2019-Ver2.3.01 REVLIMID (LENALIDOMIDE) RELAPSED/REFRACTORY OTEZLA® (apremilast) Psoriatic arthritis CC-90001 Fibrosis CC-220 Systemic lupus erythematosus Psoriasis (Japan) Ankylosing spondylitis Behçet’s disease Atopic dermatitis Ulcerative colitis Psoriasis Crohn's disease ozanimod Relapsing multiple sclerosis Ulcerativecolitis
[PRODUCT MONOGRAPH TEMPLATE Page 5of 50 WARNINGS AND PRECAUTIONS General Albumin (Human): ABRAXANE® for Injectable Suspension (paclitaxel powder for injectable suspension) (nanoparticle, albumin-bound paclitaxel) contains albumin (human), a derivative of human blood and is a 抗造血器悪性腫瘍剤ポマリスト ボルテゾミブ及びデキサメタゾン … 1 2019 年5 月22 日 報道関係各位 セルジーン株式会社 抗造血器悪性腫瘍剤ポマリスト ®、 ボルテゾミブ及びデキサメタゾンとの3 剤併用療法追加による CELGENE: A GLOBAL BIOPHARMACEUTICAL COMPANY COMMITTED TO Learn how Celgene, a global biopharmaceutical company, is committed to improving the lives of patients worldwide by delivering truly innovative and life-changing treatments. Explore the therapies for Hematology, Oncology, Inflammation and Immunology and the medical research to help people live longer, better, and healthier.VIDAZA® LOGO
These products may not be approved and/or licensed in all countries where this website is accessible. For information about Celgene products and services in countries other than the U.S., please contact the local office (as listed under the Global Network).THALOMID® LOGO
These products may not be approved and/or licensed in all countries where this website is accessible. For information about Celgene products and services in countries other than the U.S., please contact the local office (as listed under the Global Network). CELGENE REPORTS THIRD QUARTER 2019 OPERATING AND FINANCIAL October 31, 2019 Download this Press Release PDF Format (opens in new window) PDF 438 KB - Strong total revenue of $4.5 billion, increased 16% Y/Y driven by volume - INREBIC® (fedratinib) granted FDA approval in myelofibrosis; EU MAA submission expected by year-end 2019 - Expected Q4 regulatory updates include: Dec. 4, 2019 FDA PDUFA date for luspatercept in transfusion-dependent beta REVLIMID (LENALIDOMIDE) RELAPSED/REFRACTORY OTEZLA® (apremilast) Psoriatic arthritis CC-90001 Fibrosis CC-220 Systemic lupus erythematosus Psoriasis (Japan) Ankylosing spondylitis Behçet’s disease Atopic dermatitis Ulcerative colitis Psoriasis Crohn's disease ozanimod Relapsing multiple sclerosis Ulcerativecolitis
PRESS RELEASE ARCHIVE The Investor Relations website contains information about Celgene Corporation business for stockholders, potential investors, andfinancial analysts.
CELGENE CORPORATION AND ACCELERON PHARMA ANNOUNCE U.S. FDA U.S. Food and Drug Administration grants priority review for beta-thalassemia indication and sets target action date of December 4, 2019 U.S. Food and Drug Administration sets target action date of April 4, 2020 for myelodysplastic syndromes indication Luspatercept EU Marketing Authorization Application also validated Celgene Corporation (NASDAQ: CELG) and Acceleron Pharma Inc. CELGENE PROVIDES UPDATE ON GED-0301 (MONGERSEN Celgene Corporation (NASDAQ: CELG) today announced that the GED-0301 (mongersen) phase III REVOLVE trial (CD-002) in Crohn's disease (CD) and the extension trial (SUSTAIN, CD-004) will discontinue. Celgene has decided to stop the trials following an October recommendation of the Data Monitoring Committee, which assessed overall benefit/risk during a recent interim futility analysis. REVLIMID® (LENALIDOMIDA) Revlimid ® lenalidomida APRESENTAÇÕES Cada embalagem contém 21 cápsulas duras de 5 mg, 10 mg, 15 mg ou 25 mg. USO ORAL USO ADULTOACIMA DE 18 ANOS
IL CARCINOMA DEL PANCREAS IL CARCINOMA DEL PANCREAS Spesso il carcinoma del pancreas è diagnosticato allo stadio avanzato. La malattia è di solito per lungo tempo asintomatica; solamente il 7% CELGENE: A GLOBAL BIOPHARMACEUTICAL COMPANY COMMITTED TO Learn how Celgene, a global biopharmaceutical company, is committed to improving the lives of patients worldwide by delivering truly innovative and life-changing treatments. Explore the therapies for Hematology, Oncology, Inflammation and Immunology and the medical research to help people live longer, better, and healthier. CELGENE CORPORATION TO ACQUIRE JUNO THERAPEUTICS, INC SUMMIT, N.J. & SEATTLE– (BUSINESS WIRE)– Celgene Corporation (NASDAQ:CELG) and Juno Therapeutics, Inc. (NASDAQ:JUNO) today announced the signing of a definitive merger agreement in which Celgene has agreed to acquire Juno. Under the terms of the merger agreement, Celgene will pay $87 per share in cash, or a total of approximately $9 billion [PRODUCT MONOGRAPH TEMPLATE Page 1of 92 PRODUCT MONOGRAPH Pr REVLIMID® lenalidomidecapsules 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg and 25 mg Antineoplastic Agent Immunomodulatory Agent Celgene Inc. REMOTE SUPPORT PORTALSupport Portal
CELGENE CORPORATION AND ACCELERON PHARMA ANNOUNCE U.S. FDA U.S. Food and Drug Administration grants priority review for beta-thalassemia indication and sets target action date of December 4, 2019 U.S. Food and Drug Administration sets target action date of April 4, 2020 for myelodysplastic syndromes indication Luspatercept EU Marketing Authorization Application also validated Celgene Corporation (NASDAQ: CELG) and Acceleron Pharma Inc. PRODUCT MONOGRAPH INCLUDING PATIENT MEDICATION … Page 1 of 65 PRODUCT MONOGRAPH INCLUDING PATIENT MEDICATION INFORMATION Pr POMALYST® pomalidomide 1 mg, 2 mg, 3 mg and 4 mg Capsules for Oral Use Antineoplastic Agent CELGENE: A GLOBAL BIOPHARMACEUTICAL COMPANY COMMITTED TO Learn how Celgene, a global biopharmaceutical company, is committed to improving the lives of patients worldwide by delivering truly innovative and life-changing treatments. Explore the therapies for Hematology, Oncology, Inflammation and Immunology and the medical research to help people live longer, better, and healthier. CELGENE CORPORATION TO ACQUIRE JUNO THERAPEUTICS, INC SUMMIT, N.J. & SEATTLE– (BUSINESS WIRE)– Celgene Corporation (NASDAQ:CELG) and Juno Therapeutics, Inc. (NASDAQ:JUNO) today announced the signing of a definitive merger agreement in which Celgene has agreed to acquire Juno. Under the terms of the merger agreement, Celgene will pay $87 per share in cash, or a total of approximately $9 billion CELGENE: A GLOBAL BIOPHARMACEUTICAL COMPANY COMMITTED TO Learn how Celgene, a global biopharmaceutical company, is committed to improving the lives of patients worldwide by delivering truly innovative and life-changing treatments. Explore the therapies for Hematology, Oncology, Inflammation and Immunology and the medical research to help people live longer, better, and healthier. CELGENE CORPORATION TO ACQUIRE JUNO THERAPEUTICS, INC SUMMIT, N.J. & SEATTLE– (BUSINESS WIRE)– Celgene Corporation (NASDAQ:CELG) and Juno Therapeutics, Inc. (NASDAQ:JUNO) today announced the signing of a definitive merger agreement in which Celgene has agreed to acquire Juno. Under the terms of the merger agreement, Celgene will pay $87 per share in cash, or a total of approximately $9 billion [PRODUCT MONOGRAPH TEMPLATE Page 1of 92 PRODUCT MONOGRAPH Pr REVLIMID® lenalidomidecapsules 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg and 25 mg Antineoplastic Agent Immunomodulatory Agent Celgene Inc. REMOTE SUPPORT PORTALSupport Portal
CELGENE CORPORATION AND ACCELERON PHARMA ANNOUNCE U.S. FDA U.S. Food and Drug Administration grants priority review for beta-thalassemia indication and sets target action date of December 4, 2019 U.S. Food and Drug Administration sets target action date of April 4, 2020 for myelodysplastic syndromes indication Luspatercept EU Marketing Authorization Application also validated Celgene Corporation (NASDAQ: CELG) and Acceleron Pharma Inc. PRODUCT MONOGRAPH INCLUDING PATIENT MEDICATION … Page 1 of 65 PRODUCT MONOGRAPH INCLUDING PATIENT MEDICATION INFORMATION Pr POMALYST® pomalidomide 1 mg, 2 mg, 3 mg and 4 mg Capsules for Oral Use Antineoplastic Agent [PRODUCT MONOGRAPH TEMPLATE Page 5of 50 WARNINGS AND PRECAUTIONS General Albumin (Human): ABRAXANE® for Injectable Suspension (paclitaxel powder for injectable suspension) (nanoparticle, albumin-bound paclitaxel) contains albumin (human), a derivative of human blood and is a CELGENE PROVIDES UPDATE ON GED-0301 (MONGERSEN Celgene Corporation (NASDAQ: CELG) today announced that the GED-0301 (mongersen) phase III REVOLVE trial (CD-002) in Crohn's disease (CD) and the extension trial (SUSTAIN, CD-004) will discontinue. Celgene has decided to stop the trials following an October recommendation of the Data Monitoring Committee, which assessed overall benefit/risk during a recent interim futility analysis. CELGENE TO PRESENT NEW DATA FROM CLINICAL TRIALS ON ORAL UNVEIL evaluated the efficacy and safety of oral OTEZLA at 16 weeks in patients with moderate plaque psoriasis who were naïve to systemic and biologic therapy SUMMIT, N.J. -(BUSINESS WIRE)- Celgene Corporation (NASDAQ:CELG) today announced that findings from ongoing clinical trials of OTEZLA ® (apremilast), the Company's oral, selective inhibitor of phosphodiesterase 4 (PDE4), ABRAXANE® - MEDIA2.CELGENE.COM Abraxane paclitaxel (ligado à albumina) APRESENTAÇÃO . Pó liofilizado para suspensão injetável. Cada embalagem contém 1 frasco-ampola com 100 mg de paclitaxel ligado à albumina. CELGENE: A GLOBAL BIOPHARMACEUTICAL COMPANY COMMITTED TO Learn how Celgene, a global biopharmaceutical company, is committed to improving the lives of patients worldwide by delivering truly innovative and life-changing treatments. Explore the therapies for Hematology, Oncology, Inflammation and Immunology and the medical research to help people live longer, better, and healthier. CELGENE CORPORATION TO ACQUIRE JUNO THERAPEUTICS, INC SUMMIT, N.J. & SEATTLE– (BUSINESS WIRE)– Celgene Corporation (NASDAQ:CELG) and Juno Therapeutics, Inc. (NASDAQ:JUNO) today announced the signing of a definitive merger agreement in which Celgene has agreed to acquire Juno. Under the terms of the merger agreement, Celgene will pay $87 per share in cash, or a total of approximately $9 billion [PRODUCT MONOGRAPH TEMPLATE Page 1of 92 PRODUCT MONOGRAPH Pr REVLIMID® lenalidomidecapsules 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg and 25 mg Antineoplastic Agent Immunomodulatory Agent Celgene Inc. REMOTE SUPPORT PORTALSupport Portal
CELGENE CORPORATION AND ACCELERON PHARMA ANNOUNCE U.S. FDA U.S. Food and Drug Administration grants priority review for beta-thalassemia indication and sets target action date of December 4, 2019 U.S. Food and Drug Administration sets target action date of April 4, 2020 for myelodysplastic syndromes indication Luspatercept EU Marketing Authorization Application also validated Celgene Corporation (NASDAQ: CELG) and Acceleron Pharma Inc. PRODUCT MONOGRAPH INCLUDING PATIENT MEDICATION … Page 1 of 65 PRODUCT MONOGRAPH INCLUDING PATIENT MEDICATION INFORMATION Pr POMALYST® pomalidomide 1 mg, 2 mg, 3 mg and 4 mg Capsules for Oral Use Antineoplastic Agent CELGENE: A GLOBAL BIOPHARMACEUTICAL COMPANY COMMITTED TO Learn how Celgene, a global biopharmaceutical company, is committed to improving the lives of patients worldwide by delivering truly innovative and life-changing treatments. Explore the therapies for Hematology, Oncology, Inflammation and Immunology and the medical research to help people live longer, better, and healthier. CELGENE GLOBAL OFFICE LOCATIONS With locations around the world, Celgene is impacting the lives of patients with cancer, inflammatory diseases, and other serious illnesses around the world. Find here the contact information and website access to our global office locations.INVESTORS HOME
The Investor Relations website contains information about Celgene Corporation business for stockholders, potential investors, andfinancial analysts.
CELGENE CORPORATION TO ACQUIRE JUNO THERAPEUTICS, INC SUMMIT, N.J. & SEATTLE– (BUSINESS WIRE)– Celgene Corporation (NASDAQ:CELG) and Juno Therapeutics, Inc. (NASDAQ:JUNO) today announced the signing of a definitive merger agreement in which Celgene has agreed to acquire Juno. Under the terms of the merger agreement, Celgene will pay $87 per share in cash, or a total of approximately $9 billion POMALYST® PRODUCT SHOT These products may not be approved and/or licensed in all countries where this website is accessible. For information about Celgene products and services in countries other than the U.S., please contact the local office (as listed under the Global Network). [PRODUCT MONOGRAPH TEMPLATE Page 1of 92 PRODUCT MONOGRAPH Pr REVLIMID® lenalidomidecapsules 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg and 25 mg Antineoplastic Agent Immunomodulatory Agent Celgene Inc. CELGENE CORPORATION AND ACCELERON PHARMA ANNOUNCE U.S. FDAACCELERON PHARMA CAREERSACCELERON PHARMA INCACCELERON PHARMA NEWSACCELERON PHARMA RHONDA PEARSONACCELERON PHARMA SALARYACCELERON PHARMA SCAM U.S. Food and Drug Administration grants priority review for beta-thalassemia indication and sets target action date of December 4, 2019 U.S. Food and Drug Administration sets target action date of April 4, 2020 for myelodysplastic syndromes indication Luspatercept EU Marketing Authorization Application also validated Celgene Corporation (NASDAQ: CELG) and Acceleron Pharma Inc. REMOTE SUPPORT PORTALSupport Portal
CELGENE SETTLES U.S. REVLIMID® PATENT LITIGATION WITHCELGENE AUTHORIZATION REVLIMIDCELGENE REMS PROGRAMCELGENE REVLIMIDCELGENE RISKMANAGEMENT REVLIMID
Alvogen licensed to sell volume-limited amounts of generic lenalidomide in the U.S. beginning on a confidential date after the March 2022 date Celgene previously granted to Natco Alvogen also licensed to sell generic lenalidomide in the U.S. without volume limitation beginning on January 31, 2026 The earliest licensed entry of any generic lenalidomide in the U.S. continues to be March 2022 CELGENE PROVIDES UPDATE ON GED-0301 (MONGERSEN Celgene Corporation (NASDAQ: CELG) today announced that the GED-0301 (mongersen) phase III REVOLVE trial (CD-002) in Crohn's disease (CD) and the extension trial (SUSTAIN, CD-004) will discontinue. Celgene has decided to stop the trials following an October recommendation of the Data Monitoring Committee, which assessed overall benefit/risk during a recent interim futility analysis. CELGENE: A GLOBAL BIOPHARMACEUTICAL COMPANY COMMITTED TO Learn how Celgene, a global biopharmaceutical company, is committed to improving the lives of patients worldwide by delivering truly innovative and life-changing treatments. Explore the therapies for Hematology, Oncology, Inflammation and Immunology and the medical research to help people live longer, better, and healthier. CELGENE GLOBAL OFFICE LOCATIONS With locations around the world, Celgene is impacting the lives of patients with cancer, inflammatory diseases, and other serious illnesses around the world. Find here the contact information and website access to our global office locations.INVESTORS HOME
The Investor Relations website contains information about Celgene Corporation business for stockholders, potential investors, andfinancial analysts.
CELGENE CORPORATION TO ACQUIRE JUNO THERAPEUTICS, INC SUMMIT, N.J. & SEATTLE– (BUSINESS WIRE)– Celgene Corporation (NASDAQ:CELG) and Juno Therapeutics, Inc. (NASDAQ:JUNO) today announced the signing of a definitive merger agreement in which Celgene has agreed to acquire Juno. Under the terms of the merger agreement, Celgene will pay $87 per share in cash, or a total of approximately $9 billion POMALYST® PRODUCT SHOT These products may not be approved and/or licensed in all countries where this website is accessible. For information about Celgene products and services in countries other than the U.S., please contact the local office (as listed under the Global Network). [PRODUCT MONOGRAPH TEMPLATE Page 1of 92 PRODUCT MONOGRAPH Pr REVLIMID® lenalidomidecapsules 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg and 25 mg Antineoplastic Agent Immunomodulatory Agent Celgene Inc. CELGENE CORPORATION AND ACCELERON PHARMA ANNOUNCE U.S. FDAACCELERON PHARMA CAREERSACCELERON PHARMA INCACCELERON PHARMA NEWSACCELERON PHARMA RHONDA PEARSONACCELERON PHARMA SALARYACCELERON PHARMA SCAM U.S. Food and Drug Administration grants priority review for beta-thalassemia indication and sets target action date of December 4, 2019 U.S. Food and Drug Administration sets target action date of April 4, 2020 for myelodysplastic syndromes indication Luspatercept EU Marketing Authorization Application also validated Celgene Corporation (NASDAQ: CELG) and Acceleron Pharma Inc. REMOTE SUPPORT PORTALSupport Portal
CELGENE SETTLES U.S. REVLIMID® PATENT LITIGATION WITHCELGENE AUTHORIZATION REVLIMIDCELGENE REMS PROGRAMCELGENE REVLIMIDCELGENE RISKMANAGEMENT REVLIMID
Alvogen licensed to sell volume-limited amounts of generic lenalidomide in the U.S. beginning on a confidential date after the March 2022 date Celgene previously granted to Natco Alvogen also licensed to sell generic lenalidomide in the U.S. without volume limitation beginning on January 31, 2026 The earliest licensed entry of any generic lenalidomide in the U.S. continues to be March 2022 CELGENE PROVIDES UPDATE ON GED-0301 (MONGERSEN Celgene Corporation (NASDAQ: CELG) today announced that the GED-0301 (mongersen) phase III REVOLVE trial (CD-002) in Crohn's disease (CD) and the extension trial (SUSTAIN, CD-004) will discontinue. Celgene has decided to stop the trials following an October recommendation of the Data Monitoring Committee, which assessed overall benefit/risk during a recent interim futility analysis.INVESTORS HOME
The Investor Relations website contains information about Celgene Corporation business for stockholders, potential investors, andfinancial analysts.
POMALYST® PRODUCT SHOT These products may not be approved and/or licensed in all countries where this website is accessible. For information about Celgene products and services in countries other than the U.S., please contact the local office (as listed under the Global Network).THALOMID® LOGO
These products may not be approved and/or licensed in all countries where this website is accessible. For information about Celgene products and services in countries other than the U.S., please contact the local office (as listed under the Global Network). CELGENE REPORTS FOURTH QUARTER AND FULL YEAR 2018 - Exceeded 2018 top- and bottom-line guidance - 2019 guidance reflects strong operating momentum leading to double-digit top- and bottom-line growth; Reaffirming 2020 financial outlook - Advancing five late-stage assets with U.S. approvals expected through 2020; Ozanimod U.S. and EU regulatory submissions on-track for Q1:2019 Celgene Corporation (NASDAQ: CELG) reported operating results for OTEZLA-15JUL2019-VER2.3.01 Otexla Safety Data Sheet. Otezla-15Jul2019-Ver2.3.01 EVENTS & PRESENTATIONS ARCHIVE Celgene undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events or otherwise. Additional factors that could cause results to differ materially from those described in the forward-looking statements can be found in Celgene's Annual Report Form 10-K and the company's other PASSION, INNOVATION, COURAGE n 1992, Celgene licensed the patent for thalidomide, a controversial anti-nausea drug and sleep aid that was withdrawn from markets around the world in the early CELGENE PROVIDES UPDATE ON GED-0301 (MONGERSEN Celgene Corporation (NASDAQ: CELG) today announced that the GED-0301 (mongersen) phase III REVOLVE trial (CD-002) in Crohn's disease (CD) and the extension trial (SUSTAIN, CD-004) will discontinue. Celgene has decided to stop the trials following an October recommendation of the Data Monitoring Committee, which assessed overall benefit/risk during a recent interim futility analysis. CELGENE IN COLLABORATION WITH ASTRAZENECA ANNOUNCE Program starting with four studies of durvalumab and combination therapies across multiple hematologic disorders Celgene Corporation (NASDAQ:CELG) and AstraZeneca (NYSE:AZN), today announced the initiation of the FUSION clinical development program of durvalumab (MEDI4736), an investigational human monoclonal antibody directed against programmed cell death ligand 1 (PD SIZE/CLASSIFICATION SELF-CERTIFICATION FORM Small and Diverse Business Classifications. Definition of Large Business: Large Business: According to the federal government, this definition may vary based on your industry; for our purposes, we are referring to businesses that do not meet the size standard list at 13 CFR Part 121.201 via Our Medicines Contact UsCareers _ _
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Bristol Myers Squibb’s new oral treatment option is now approved for appropriate patients with ulcerative colitis.OUR R&D TEAM >
Learn more about the backgrounds, scientific pursuits and personal interests of members of our research team. PATIENT & EMPLOYEE STORIES > We invite you to meet some of our people — employees who embody and give expression to our mission, and patients whose determination fuels and energizes our work. Their words are personal and powerful, and together, they help tell the Bristol Myers Squibbstory.
LIFE & SCIENCE STORIES A subset of BMS.com, Life & Science Stories is where we share the work our global community of colleagues are doing around the world to help patients and advance scientific innovation.Learn More >
May 26, 2021 World Multiple Sclerosis Day 2021: a Q&A with Cathy Trzaskawka and Richard Nieman _ _ May 25, 2021 Harnessing translational medicine to guide drug discovery and development _ _ May 19, 2021 Fighting the stigma: How candid conversations may help men facing cancer _ _ May 19, 2021 News & Perspectives Are you familiar with AFib symptoms and the increased risk of stroke associated with thecondition? _ _
May 19, 2021 Science Understanding the potential of LAG-3 _ _ May 18, 2021 News & Perspectives Patient engagement and diversity in clinical trials _ _SURVIVORSHIP TODAY
Emmy winner Sterling K. Brown explores cancer survivorship during aglobal pandemic.
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May 28, 2021
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