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07 Aug 2024
// BUSINESSWIRE
15 Jul 2024
// PR NEWSWIRE
https://www.prnewswire.com/news-releases/sumitomo-pharma-announces-that-dsp-5336-has-received-fda-fast-track-designation-for-the-treatment-of-relapsed-or-refractory-acute-myeloid-leukemia-302196812.html
27 Jun 2024
// FIERCE PHARMA
https://www.fiercepharma.com/pharma/following-sweeping-us-layoffs-amid-revenue-decline-sumitomo-pharmas-new-head-weighs-japan
14 Jun 2024
// PR NEWSWIRE
https://www.prnewswire.com/news-releases/sumitomo-pharma-presents-new-clinical-data-on-dsp-5336-at-the-european-hematology-association-2024-congress-302173004.html
22 May 2024
// ENDPTS
https://endpts.com/sumitomo-and-japan-national-institutes-universal-influenza-vaccine-enters-clinical-trials/
13 May 2024
// PR NEWSWIRE
https://www.prnewswire.com/news-releases/sumitomo-pharma-announces-fda-acceptance-of-supplemental-new-drug-application-for-vibegron-in-men-with-overactive-bladder-symptoms-receiving-pharmacological-therapy-for-benign-prostatic-hyperplasia-302143418.html
Details:
TWYMEEG (imeglimin hydrochloride), enhances insulin action by inhibiting hepatic glucose output and improving insulin signalling in both liver and skeletal muscle, in type 2 diabetes patients.
Lead Product(s): Imeglimin Hydrochloride
Therapeutic Area: Endocrinology Brand Name: Twymeeg
Study Phase: Phase IVProduct Type: Small molecule
Sponsor: Poxel
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable August 07, 2024
Lead Product(s) : Imeglimin Hydrochloride
Therapeutic Area : Endocrinology
Highest Development Status : Phase IV
Partner/Sponsor/Collaborator : Poxel
Deal Size : Not Applicable
Deal Type : Not Applicable
Sumitomo And Poxel Announce TWYMEEG® Study Results For Type 2 Diabetes Treatment
Details : TWYMEEG (imeglimin hydrochloride), enhances insulin action by inhibiting hepatic glucose output and improving insulin signalling in both liver and skeletal muscle, in type 2 diabetes patients.
Brand Name : Twymeeg
Molecule Type : Small molecule
Upfront Cash : Not Applicable
August 07, 2024
Details:
DSP-5336, an Investigational menin and mixed-lineage leukemia inhibitor, is being evaluated in patients with relapsed or refractory acute myeloid leukemia with a KMT2A rearrangement.
Lead Product(s): Enzomenib
Therapeutic Area: Oncology Brand Name: DSP-5336
Study Phase: Phase I/ Phase IIProduct Type: Small molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable July 15, 2024
Lead Product(s) : Enzomenib
Therapeutic Area : Oncology
Highest Development Status : Phase I/ Phase II
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Sumitomo Pharma’s DSP-5336 Receives FDA Fast Track for Acute Myeloid Leukemia
Details : DSP-5336, an Investigational menin and mixed-lineage leukemia inhibitor, is being evaluated in patients with relapsed or refractory acute myeloid leukemia with a KMT2A rearrangement.
Brand Name : DSP-5336
Molecule Type : Small molecule
Upfront Cash : Not Applicable
July 15, 2024
Details:
fH1/DSP-0546LP is a vaccine candidate, specifically activates TLR7, being investigated for influenza.
Lead Product(s): fH1,DSP-0546LP
Therapeutic Area: Infections and Infectious Diseases Brand Name: fH1
Study Phase: Phase IProduct Type: Vaccine
Sponsor: National Institutes of Biomedical Innovation, Health and nutrition
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable May 22, 2024
Lead Product(s) : fH1,DSP-0546LP
Therapeutic Area : Infections and Infectious Diseases
Highest Development Status : Phase I
Partner/Sponsor/Collaborator : National Institutes of Biomedical Innovation, Health and nutrition
Deal Size : Not Applicable
Deal Type : Not Applicable
Sumitomo and Japan National Institute's universal influenza vaccine enters clinical trials
Details : fH1/DSP-0546LP is a vaccine candidate, specifically activates TLR7, being investigated for influenza.
Brand Name : fH1
Molecule Type : Vaccine
Upfront Cash : Not Applicable
May 22, 2024
Details:
Gemtesa (vibegron) is a beta-3 adrenergic receptor agonist for treating male overactive bladder (OAB) with benign prostatic hyperplasia.
Lead Product(s): Vibegron
Therapeutic Area: Urology Brand Name: Gemtesa
Study Phase: Phase IIIProduct Type: Small molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable May 13, 2024
Sumitomo Pharma’s Vibegron Supplemental NDA Accepted By FDA
Details : Gemtesa (vibegron) is a beta-3 adrenergic receptor agonist for treating male overactive bladder (OAB) with benign prostatic hyperplasia.
Brand Name : Gemtesa
Molecule Type : Small molecule
Upfront Cash : Not Applicable
May 13, 2024
Details:
Under the license agreement, Otsuka holds exclusive rights to develop, manufacture, and commercialize SEP-363856 (ulotaront), TAAR1 agonist. It is being evaluated with the patient for Schizophrenia.
Lead Product(s): Ulotaront
Therapeutic Area: Psychiatry/Psychology Brand Name: SEP-363856
Study Phase: Phase IIIProduct Type: Small molecule
Sponsor: Otsuka Pharmaceutical
Deal Size: $30.0 million Upfront Cash: Undisclosed
Deal Type: Licensing Agreement March 15, 2024
Lead Product(s) : Ulotaront
Therapeutic Area : Psychiatry/Psychology
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Otsuka Pharmaceutical
Deal Size : $30.0 million
Deal Type : Licensing Agreement
Otsuka and Sumitomo Revise License Agreement
Details : Under the license agreement, Otsuka holds exclusive rights to develop, manufacture, and commercialize SEP-363856 (ulotaront), TAAR1 agonist. It is being evaluated with the patient for Schizophrenia.
Brand Name : SEP-363856
Molecule Type : Small molecule
Upfront Cash : Undisclosed
March 15, 2024
Details:
Orgovyx (relugolix) is a nonpeptide GnRH receptor antagonist. It is launched in Canada for testosterone suppression in patients with advanced prostate cancer.
Lead Product(s): Relugolix
Therapeutic Area: Oncology Brand Name: Orgovyx
Study Phase: ApprovedProduct Type: Small molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable March 12, 2024
Sumitomo Launches ORGOVYX® in Canada for Prostate Cancer Treatment
Details : Orgovyx (relugolix) is a nonpeptide GnRH receptor antagonist. It is launched in Canada for testosterone suppression in patients with advanced prostate cancer.
Brand Name : Orgovyx
Molecule Type : Small molecule
Upfront Cash : Not Applicable
March 12, 2024
Details:
ORGOVYX (relugolix), is the first and only oral gonadotropin-releasing hormone (GnRH) receptor antagonist, for the treatment of men with advanced prostate cancer.
Lead Product(s): Relugolix
Therapeutic Area: Oncology Brand Name: Orgovyx
Study Phase: ApprovedProduct Type: Small molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable October 24, 2023
Sumitomo Pharma Announces Authorization in Canada of Orgovyx for Treatment Prostate Cancer
Details : ORGOVYX (relugolix), is the first and only oral gonadotropin-releasing hormone (GnRH) receptor antagonist, for the treatment of men with advanced prostate cancer.
Brand Name : Orgovyx
Molecule Type : Small molecule
Upfront Cash : Not Applicable
October 24, 2023
Details:
Orogvyx (relugolix), is the first and only oral gonadotropin-releasing hormone (GnRH) receptor antagonist, for the treatment of men with advanced prostate cancer.
Lead Product(s): Relugolix
Therapeutic Area: Oncology Brand Name: Orgovyx
Study Phase: ApprovedProduct Type: Small molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable October 23, 2023
Sumitomo Pharma Announces Authorization in Canada of ORGOVYX® (relugolix) for the Treatment of Me...
Details : Orogvyx (relugolix), is the first and only oral gonadotropin-releasing hormone (GnRH) receptor antagonist, for the treatment of men with advanced prostate cancer.
Brand Name : Orgovyx
Molecule Type : Small molecule
Upfront Cash : Not Applicable
October 23, 2023
Details:
Under the agreement, Veneno will conduct a program to obtain functional peptides (DRPs) for ion channels targeted by Sumitomo Pharma using Veneno Technologies' next-generation peptide discovery technology, the PERISS™ method (intra-periplasm secretion and selection).
Lead Product(s): Undisclosed
Therapeutic Area: Technology Brand Name: Undisclosed
Study Phase: DiscoveryProduct Type: Peptide
Recipient: Veneno Technologies
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Agreement April 18, 2023
Lead Product(s) : Undisclosed
Therapeutic Area : Technology
Highest Development Status : Discovery
Recipient : Veneno Technologies
Deal Size : Undisclosed
Deal Type : Agreement
Details : Under the agreement, Veneno will conduct a program to obtain functional peptides (DRPs) for ion channels targeted by Sumitomo Pharma using Veneno Technologies' next-generation peptide discovery technology, the PERISS™ method (intra-periplasm secretion ...
Brand Name : Undisclosed
Molecule Type : Peptide
Upfront Cash : Undisclosed
April 18, 2023
Details:
The agreement includes the marketing alliance for JR-051 (agalsidase beta BS), a biosimilar of Fabrazyme, a therapeutic enzyme, being sold by JCR for the treatment of Fabry disease.
Lead Product(s): Agalsidase Beta
Therapeutic Area: Genetic Disease Brand Name: JR-051
Study Phase: ApprovedProduct Type: Cell and Gene therapy
Recipient: JCR Pharmaceuticals
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Agreement March 01, 2022
Lead Product(s) : Agalsidase Beta
Therapeutic Area : Genetic Disease
Highest Development Status : Approved
Recipient : JCR Pharmaceuticals
Deal Size : Undisclosed
Deal Type : Agreement
Details : The agreement includes the marketing alliance for JR-051 (agalsidase beta BS), a biosimilar of Fabrazyme, a therapeutic enzyme, being sold by JCR for the treatment of Fabry disease.
Brand Name : JR-051
Molecule Type : Cell and Gene therapy
Upfront Cash : Undisclosed
March 01, 2022
RLD : Yes
TE Code :
ESTRADIOL; NORETHINDRONE ACETATE; RELUGOLIX
Dosage Form : TABLET; ORAL
Proprietary Name : MYFEMBREE
Dosage Strength : 1MG;0.5MG;40MG
Approval Date : 2021-05-26
Application Number : 214846
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ORGOVYX
Dosage Strength : 120MG
Approval Date : 2020-12-18
Application Number : 214621
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
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