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Find Drugs in Development News & Deals for Umeclidinium Bromide

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Details:

The Company now anticipates it will approach breakeven cash flow in the second half of 2022 without the cash flows from its interest in GSK's Trelegy Ellipta (fluticasone furoate) royalties, driven by disciplined spending within R&D and the growth of YUPELRI®.


Lead Product(s): Fluticasone Furoate,Umeclidinium Bromide,Vilanterol Trifenatate

Therapeutic Area: Pulmonary/Respiratory Diseases Product Name: Trelegy Ellipta

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Royalty Pharma

Deal Size: $1,550.0 million Upfront Cash: $1,100.0 million

Deal Type: Divestment July 13, 2022

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  • Development Update

Details:

Trelegy Ellipta (fluticasone furoate) is a glucocorticoid receptor binder which is approved in combination with umeclidinium & vilanterol for the treatment of chronic obstructive pulmonary disease.


Lead Product(s): Fluticasone Furoate,Umeclidinium Bromide,Vilanterol Trifenatate

Therapeutic Area: Pulmonary/Respiratory Diseases Product Name: Trelegy Ellipta

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 26, 2022

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  • Development Update

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Trelegy Ellipta (fluticasone furoate) is a glucocorticoid receptor binder which is being evaluated in phase 4 clinical trials in combination with umeclidinium & vilanterol for the treatment of chronic obstructive pulmonary disease.


Lead Product(s): Fluticasone Furoate,Umeclidinium Bromide,Vilanterol Trifenatate

Therapeutic Area: Pulmonary/Respiratory Diseases Product Name: Trelegy Ellipta

Highest Development Status: Phase IVProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable May 10, 2021

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  • Development Update

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The European Union’s healthcare regulator the European Medicines Agency (EMA) has decided against a label expansion for GlaxoSmithKline (GSK)’s drug Trelegy Ellipta (fluticasone furoate/umeclidinium/vilanterol) to include asthma.


Lead Product(s): Fluticasone Furoate,Umeclidinium Bromide,Vilanterol Trifenatate

Therapeutic Area: Pulmonary/Respiratory Diseases Product Name: Trelegy Ellipta

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 01, 2021

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  • Development Update

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FDA has approved a new indication for Trelegy Ellipta (fluticasone furoate / umeclidinium / vilanterol ‘FF/UMEC/VI’) for the treatment of asthma in patients aged 18 years and older adding to its current license for use in patients with COPD.


Lead Product(s): Fluticasone Furoate,Umeclidinium Bromide,Vilanterol Trifenatate

Therapeutic Area: Pulmonary/Respiratory Diseases Product Name: Trelegy Ellipta

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 09, 2020

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  • Development Update

Details:

Trelegy Ellipta (fluticasone furoate) is a glucocorticoid receptor binder which is under phase 3 clinical development in combination with umeclidinium & vilanterol for the treatment of adult patients with Asthma.


Lead Product(s): Fluticasone Furoate,Umeclidinium Bromide,Vilanterol Trifenatate

Therapeutic Area: Pulmonary/Respiratory Diseases Product Name: Trelegy Ellipta

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 27, 2020

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