Inabata Inabata

X

Find Radio Compass News for Luspatercept

PharmaCompass
API SUPPLIERS
API Suppliers

API Suppliers

0

US DMFs Filed

US DMFs Filed

0

CEP/COS Certifications

CEP/COS Certifications

0

JDMFs Filed

JDMFs Filed

0

EU WC

EU WC

0

Listed Suppliers

Listed Suppliers

0

API REF. PRICE (USD / KG)

0

INTERMEDIATES

0

DOSSIERS // FDF
USA (Orange Book)

USA (Orange Book)

Europe

Europe

0

Canada

Canada

Australia

Australia

0

South Africa

South Africa

0

Uploaded Dossiers

Uploaded Dossiers

0

GLOBAL SALES (USD Million)

U.S. Medicaid

0

Annual Reports

EXCIPIENTS

0

PATENTS & EXCLUSIVITIES

USFDA Orange Book Patents

0

USFDA Exclusivities

0

DIGITAL CONTENT

Blog #PharmaFlow

0

News

REF STANDARD

EDQM

0

USP

0

JP

0

Other Listed Suppliers

0

SERVICES

0

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=761136

FDA
16 May 2024

https://endpts.com/ahead-of-likely-approval-icer-finds-gerons-imetelstat-is-not-cost-effective-at-250000-annually/

Lia DeGroot ENDPTS
09 May 2024

https://www.businesswire.com/news/home/20240402231542/en

BUSINESSWIRE
02 Apr 2024

https://www.indianpharmapost.com/drug-approval/ec-expands-reblozyls-approval-for-treatment-of-myelodysplastic-syndromes-15475

INDIANPHARMAPOST
02 Apr 2024

https://www.businesswire.com/news/home/20240221131768/en

BUSINESSWIRE
23 Feb 2024

https://www.businesswire.com/news/home/20231208530578/en

BUSINESSWIRE
09 Dec 2023

https://www.onclive.com/view/fda-approval-insights-first-line-luspatercept-for-anemia-in-lower-risk-mds

ONCLIVE
05 Oct 2023

https://news.bms.com/news/details/2023/U.S.-FDA-Approves-Bristol-Myers-Squibbs-Reblozyl-luspatercept-aamt-as-First-Line-Treatment-of-Anemia-in-Adults-with-Lower-Risk-Myelodysplastic-Syndromes-MDS-Who-May-Require-Transfusions/default.aspx

PRESS RELEASE
30 Aug 2023

https://www.globenewswire.com/news-release/2023/08/29/2733042/0/en/European-Commission-approves-Roche-s-Evrysdi-for-babies-under-two-months-old-with-spinal-muscular-atrophy-SMA.html

GLOBENEWSWIRE
30 Aug 2023

https://www.businesswire.com/news/home/20230622657196/en

BUSINESSWIRE
28 Aug 2023

https://endpts.com/bristol-myers-details-phiii-win-in-first-line-test-of-reblozyl-for-reducing-transfusions-in-myelodysplastic-syndrome/

Ryan Cross ENDPTS
26 May 2023

https://www.businesswire.com/news/home/20230524005878/en

BUSINESSWIRE
25 May 2023

https://www.fiercepharma.com/pharma/bristol-myers-4b-plan-reblozyl-takes-shape-blood-cancer-anemia-one-caveat

Angus Liu FIERCE PHARMA
25 May 2023

https://www.businesswire.com/news/home/20230429005037/en

BUSINESSWIRE
01 May 2023

https://www.businesswire.com/news/home/20230501005182/en

BUSINESSWIRE
01 May 2023

https://news.bms.com/news/corporate-financial/2023/U.S.-FDA-Accepts-for-Priority-Review-Supplemental-Biologics-License-Application-and-EMA-Validates-Application-for-Reblozyl-luspatercept-aamt-as-First-Line-Treatment-of-Anemia-in-Adults-with-Lower-Risk-Myelodysplastic-Syndromes-MDS/default.aspx

PRESS RELEASE
01 May 2023

https://www.businesswire.com/news/home/20230302005889/en/Bristol-Myers-Squibb-Receives-European-Commission-Approval-of-Reblozyl%C2%AE-luspatercept-for-Anemia-in-Adult-Patients-with-Non-Transfusion-Dependent-Beta-Thalassemia

BUSINESSWIRE
04 Mar 2023

https://www.businesswire.com/news/home/20230126005825/en

BUSINESSWIRE
28 Jan 2023

https://www.fiercepharma.com/pharma/bristol-myers-squibbs-reblozyl-scores-top-line-treat-positive-results-phase-3-trial

Zoey Becker FIERCEPHARMA
01 Nov 2022

https://www.europeanpharmaceuticalreview.com/news/175867/new-therapy-for-anaemic-myelodysplastic-cancer-patients/

Catherine Eckford EUROPEANPHARMACEUTICALREVIEW
01 Nov 2022

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=761136

FDA
08 Jul 2022

https://www.businesswire.com/news/home/20220603005473/en

BUSINESSWIRE
03 Jun 2022

https://www.forbes.com/sites/greatspeculations/2022/04/28/what-to-expect-from-bristol-myers-squibb-stock-after-q1-results/?sh=1516cc674893

FORBES
28 Apr 2022

https://www.businesswire.com/news/home/20220324006050/en

BUSINESSWIRE
25 Mar 2022

https://www.prnewswire.com/news-releases/european-hematology-association---above-and-beyond-luspatercept-is-efficacious-and-well-tolerated-in-patients-with-non-transfusion-dependent--thalassemia-301310111.html

PRNEWSWIRE
11 Jun 2021

https://www.prnewswire.com/news-releases/european-hematology-association-beyond-le-luspatercept-est-efficace-et-bien-tolere-chez-les-patients-atteints-de-beta-thalassemie-non-dependante-de-la-transfusion-867240609.html

PRNEWSWIRE
11 Jun 2021

https://www.businesswire.com/news/home/20210611005039/en

BUSINESSWIRE
11 Jun 2021

https://www.prnewswire.com/news-releases/european-hematology-association---above-and-beyond-luspatercept-is-efficacious-and-well-tolerated-in-patients-with-non-transfusion-dependent--thalassemia-301310111.html

PRNEWSWIRE
11 Jun 2021

https://www.prnewswire.com/news-releases/european-hematology-association-beyond-le-luspatercept-est-efficace-et-bien-tolere-chez-les-patients-atteints-de-beta-thalassemie-non-dependante-de-la-transfusion-867240609.html

PRNEWSWIRE
11 Jun 2021

https://www.businesswire.com/news/home/20210611005039/en

BUSINESSWIRE
11 Jun 2021

https://www.businesswire.com/news/home/20210216005710/en

BUSINESSWIRE
16 Feb 2021

https://www.biospace.com/article/releases/health-canada-approves-reblozyl-luspatercept-new-class-of-treatment-for-adult-patients-living-with-myelodysplastic-syndromes/?s=85

BIOSPACE
16 Feb 2021

https://www.businesswire.com/news/home/20201104005596/en/Acceleron-Announces-REBLOZYL%C2%AE-luspatercept-aamt-Virtual-Presentations-at-the-62nd-American-Society-of-Hematology-Annual-Meeting

BUSINESSWIRE
04 Nov 2020

https://www.businesswire.com/news/home/20200929005333/en

BUSINESSWIRE
29 Sep 2020

https://www.biospace.com/article/health-canada-approves-reblozyl-new-class-of-treatment-for-adult-patients-living-with-beta-thalassemia/

BIOSPACE
29 Sep 2020

https://www.ema.europa.eu/en/documents/assessment-report/reblozyl-epar-public-assessment-report_en.pdf

EMA
08 Jul 2020

http://www.pharmatimes.com/news/ec_clears_new_class_of_anaemia_therapy_1343242

Selina McKee PHARMATIMES
29 Jun 2020

https://www.businesswire.com/news/home/20200626005247/en

BUSINESSWIRE
25 Jun 2020

https://www.businesswire.com/news/home/20200520005073/en

BUSINESSWIRE
20 May 2020

https://www.businesswire.com/news/home/20200430005886/en

BUSINESSWIRE
30 Apr 2020

https://news.bms.com/press-release/corporatefinancial-news/us-food-and-drug-administration-fda-approves-reblozyl-luspater

PRESS RELEASE
07 Apr 2020

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=761136

FDA
06 Apr 2020

https://news.bms.com/press-release/rd-news/new-england-journal-medicine-publishes-results-pivotal-phase-3-believe-trial-r

PRESS RELEASE
26 Mar 2020

https://www.businesswire.com/news/home/20200326005054/en

BUSINESSWIRE
26 Mar 2020

https://www.fda.gov/advisory-committees/updated-public-participation-information-december-18-2019-meeting-oncologic-drugs-advisory-committee

FDA
16 Dec 2019

https://www.businesswire.com/news/home/20191206005374/en

BUSINESS WIRE
06 Dec 2019

https://www.fiercepharma.com/marketing/can-biohaven-challenge-allergan-abbvie-goliath-migraine-ceo-coric-thinks-so

 Eric Sagonowsky FIERCE PHARMA
03 Dec 2019

https://www.fiercepharma.com/pharma/blockbuster-balance-celgene-s-reblozyl-faces-fda-committee-for-mds

K. Blankenship  FIERCE PHARMA
03 Dec 2019

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=761136

FDA
13 Nov 2019

https://www.prnewswire.com/news-releases/fda-approves-first-therapy-to-treat-patients-with-rare-blood-disorder-300954846.html

PR NEWSWIRE
08 Nov 2019
Ask Us for Pharmaceutical Supplier and Partner
Ask Us, Find A Supplier / Partner
No Commissions, No Strings Attached, Get Connected for FREE

What are you looking for?

How can we help you?

The request can't be empty

Please read our Privacy Policy carefully

You must agree to the privacy policy

The name can't be empty
The company can't be empty.
The email can't be empty Please enter a valid email.
The mobile can't be empty
Post Enquiry
POST ENQUIRY