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24 Mar 2021
// REUTERS
https://www.reuters.com/article/us-health-coronavirus-brazil-sputnik/brazil-could-approve-russian-coronavirus-vaccine-in-days-says-pharmaceutical-firm-idUSKBN2BF34V

http://portal.anvisa.gov.br/wps/content/anvisa+portal/anvisa/sala+de+imprensa/menu+-+noticias+anos/2015/medicamento+standor+tem+lote+suspenso+pela+anvisa
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Details:
Documents supporting drugmaker Uniao Quimica’s application for emergency use of Sputnik V have been returned to the company because they did not meet its minimum criteria.
Lead Product(s): Gam-COVID-Vac
Therapeutic Area: Infections and Infectious Diseases Brand Name: Sputnik V
Study Phase: Phase IIIProduct Type: Vaccine
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable January 17, 2021

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Lead Product(s) : Gam-COVID-Vac
Therapeutic Area : Infections and Infectious Diseases
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Brazilian Approval of Sputnik V Vaccine Delayed by Missing Data
Details : Documents supporting drugmaker Uniao Quimica’s application for emergency use of Sputnik V have been returned to the company because they did not meet its minimum criteria.
Product Name : Sputnik V
Product Type : Vaccine
Upfront Cash : Inapplicable
January 17, 2021

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Sodium Heparin is a Other Small Molecule drug candidate, which is currently being evaluated in phase I clinical studies for the treatment of undefined medical condition.
Lead Product(s): Heparin Sodium
Therapeutic Area: Undisclosed Brand Name: Undisclosed
Study Phase: Phase IProduct Type: Miscellaneous
Sponsor: Buranello e Rodrigues Consultoria
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable April 24, 2017

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Lead Product(s) : Heparin Sodium
Therapeutic Area : Undisclosed
Highest Development Status : Phase I
Partner/Sponsor/Collaborator : Buranello e Rodrigues Consultoria
Deal Size : Inapplicable
Deal Type : Inapplicable
Study With Heparin Sodium in Intravenous Administration
Details : Sodium Heparin is a Other Small Molecule drug candidate, which is currently being evaluated in phase I clinical studies for the treatment of undefined medical condition.
Product Name : Undisclosed
Product Type : Miscellaneous
Upfront Cash : Inapplicable
April 24, 2017

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Details:
Amblyomin-X is a Other Large Molecule drug candidate, which is currently being evaluated in phase I clinical studies for the treatment of Neoplasms.
Lead Product(s): Amblyomin-X
Therapeutic Area: Oncology Brand Name: Undisclosed
Study Phase: Phase IProduct Type: Protein
Sponsor: Buranello e Rodrigues Consultoria
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable April 19, 2017

Study of Amblyomin-X in Advanced Solid Tumor
Details : Amblyomin-X is a Other Large Molecule drug candidate, which is currently being evaluated in phase I clinical studies for the treatment of Neoplasms.
Product Name : Undisclosed
Product Type : Protein
Upfront Cash : Inapplicable
April 19, 2017

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Details:
Sodium Heparin is a Other Small Molecule drug candidate, which is currently being evaluated in phase I clinical studies for the treatment of undefined medical condition.
Lead Product(s): Heparin Sodium
Therapeutic Area: Undisclosed Brand Name: Undisclosed
Study Phase: Phase IProduct Type: Miscellaneous
Sponsor: Buranello e Rodrigues Consultoria
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable April 13, 2017

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Lead Product(s) : Heparin Sodium
Therapeutic Area : Undisclosed
Highest Development Status : Phase I
Partner/Sponsor/Collaborator : Buranello e Rodrigues Consultoria
Deal Size : Inapplicable
Deal Type : Inapplicable
Study With Heparin Sodium in Subcutaneous Administration
Details : Sodium Heparin is a Other Small Molecule drug candidate, which is currently being evaluated in phase I clinical studies for the treatment of undefined medical condition.
Product Name : Undisclosed
Product Type : Miscellaneous
Upfront Cash : Inapplicable
April 13, 2017

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Details:
Levonorgestrel is a Hormone drug candidate, which is currently being evaluated in phase III clinical studies for the treatment of Menstruation Disturbances.
Lead Product(s): Levonorgestrel,Ethinyl Estradiol
Therapeutic Area: Obstetrics/Gynecology (Women’s Health) Brand Name: Undisclosed
Study Phase: Phase IIIProduct Type: Hormone
Recipient: Azidus
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable November 29, 2011

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Lead Product(s) : Levonorgestrel,Ethinyl Estradiol
Therapeutic Area : Obstetrics/Gynecology (Women’s Health)
Highest Development Status : Phase III
Recipient : Azidus
Deal Size : Inapplicable
Deal Type : Inapplicable
Evaluation of Ciclo 21® Effect (Levonorgestrel + Ethinyl Estradiol) Compared to Nordette®.
Details : Levonorgestrel is a Hormone drug candidate, which is currently being evaluated in phase III clinical studies for the treatment of Menstruation Disturbances.
Product Name : Undisclosed
Product Type : Hormone
Upfront Cash : Inapplicable
November 29, 2011

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Regulatory Info :
Registration Country : Brazil
Clobutinol HCl; Doxylamine Succinate
Uniao Quimica Farmaceutica Nacional
Dosage Form : Oral Solution; Oral Solu...
Brand Name : Hytós Plus
Dosage Strength : 48MG/15ML; 9MG/15ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Brazil

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Regulatory Info :
Registration Country : Brazil
clobutinol hydrochloride; Doxylamine Succinate
Uniao Quimica Farmaceutica Nacional
Dosage Form : Syrup; Syrup
Brand Name : Hytós Plus
Dosage Strength : 4MG/100ML; 0.75MG/100M...
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Brazil

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
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Regulatory Info :
Registration Country : Brazil
Clobutinol HCl; Doxylamine Succinate
Uniao Quimica Farmaceutica Nacional
Dosage Form : Oral Solution; Oral Solution
Brand Name : Hytós Plus
Dosage Strength : 48MG/15ML; 9MG/15ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Brazil

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info :
Registration Country : Brazil
clobutinol hydrochloride; Doxylamine Succinate
Uniao Quimica Farmaceutica Nacional
Dosage Form : Syrup; Syrup
Brand Name : Hytós Plus
Dosage Strength : 4MG/100ML; 0.75MG/100M...
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Brazil

FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]ABOUT THIS PAGE