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November 8, 2021
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https://www.merck.com/news/merck-announces-receipt-of-antitrust-clearance-in-germany-and-austria-relating-to-tender-offer-to-acquire-acceleron-pharma-inc/
Merck Announces Receipt of Antitrust Clearance in Germany and Austria Relating to Tender Offer to Acquire Acceleron Pharma Inc.
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November 4, 2021
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https://www.merck.com/news/merck-and-ridgebacks-molnupiravir-an-oral-covid-19-antiviral-medicine-receives-first-authorization-in-the-world/
Merck and Ridgeback’s Molnupiravir, an Oral COVID-19 Antiviral Medicine, Receives First Authorization in the World
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October 31, 2021
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https://www.merck.com/news/new-research-for-keytruda-pembrolizumab-at-society-for-melanoma-research-smr-2021-congress-reinforces-mercks-commitment-to-patients-with-melanoma-across-stages-of-disease/
New Research for KEYTRUDA® (pembrolizumab) at Society for Melanoma Research (SMR) 2021 Congress Reinforces Merck’s Commitment to Patients With Melanoma Across Stages of Disease
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October 29, 2021
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https://www.merck.com/news/merck-announces-withdrawal-and-refiling-under-the-hart-scott-rodino-act-and-extension-of-tender-offer-to-acquire-acceleron-pharma-inc/
Merck Announces Withdrawal and Refiling under the Hart-Scott-Rodino Act and Extension of Tender Offer to Acquire Acceleron Pharma Inc.
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October 28, 2021
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Merck Announces Third-Quarter 2021 Financial Results
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October 27, 2021
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https://www.merck.com/news/merck-presents-new-data-from-ongoing-phase-2b-clinical-trial-evaluating-efficacy-and-safety-of-investigational-islatravir-in-combination-with-doravirine-through-144-weeks-for-hiv-1-treatment-at-eacs-2/
Merck Presents New Data from Ongoing Phase 2b Clinical Trial Evaluating Efficacy and Safety of Investigational Islatravir in Combination With Doravirine Through 144 Weeks for HIV-1 Treatment at EACS 2021
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September 23, 2021
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Merck Announces Settlement and License Agreement Resolving Pneumococcal Conjugate Vaccine Patent Litigation
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September 21, 2021
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Building Sustainable Value for our Business and Society
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July 9, 2021
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Merck Statement on Clinical Data for Molnupiravir Generated by Hetero in India
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April 29, 2021
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https://www.merck.com/news/fdas-oncologic-drugs-advisory-committee-to-discuss-three-indications-for-keytruda-pembrolizumab-during-meetings-focused-on-accelerated-approvals-2/
Merck Provides Update on FDA’s Oncologic Drugs Advisory Committee (ODAC) Meetings on April 28-29, 2021
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March 11, 2021
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https://www.merck.com/news/fdas-oncologic-drugs-advisory-committee-to-discuss-three-indications-for-keytruda-pembrolizumab-during-meetings-focused-on-accelerated-approvals/
FDA’s Oncologic Drugs Advisory Committee to Discuss Three Indications for KEYTRUDA® (pembrolizumab) During Meetings Focused on Accelerated Approvals
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February 9, 2021
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https://www.merck.com/news/merck-announces-outcome-of-oncologic-drugs-advisory-committee-odac-for-keytruda-pembrolizumab-for-treatment-of-patients-with-high-risk-early-stage-triple-negative-breast-cancer-tnbc/
Merck Announces Outcome of Oncologic Drugs Advisory Committee (ODAC) for KEYTRUDA® (pembrolizumab) for Treatment of Patients With High-Risk Early-Stage Triple-Negative Breast Cancer (TNBC)
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