https://www.jnj.com/media-center/press-releases/janssen-submits-new-drug-application-to-u-s-fda-seeking-approval-of-investigational-single-tablet-combination-therapy-of-macitentan-and-tadalafil-for-treatment-of-patients-with-pulmonary-arterial-hypertension-pah
This is the first and only single tablet combination therapy application to be submitted for review in the U.S. for this rare, progressive disease If approved,...
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https://www.psychiatrictimes.com/view/fda-clears-investigational-new-drug-application-for-tnx-102-sl-for-treatment-of-major-depressive-disorder
Nov 24, 2025 - Psychiatric Times is the connection to Psychiatry and Mental Health, featuring clinical updates, expert views, and research news in multimedia formats.
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https://www.takeda.com/en-us/newsroom/news-releases/2011/takeda-resubmits-new-drug-applications-in-the-us-for-investigational-type-2-diabetes-therapies-alogliptin-and-the-fixed-dose-combination-alogliptinpioglitazone/
Takeda Resubmits New Drug Applications in the U.S. for Investigational Type 2 Diabetes Therapies Alogliptin and the Fixed-Dose Combination...
new drug applicationsin thetakeda
https://www.technologynetworks.com/neuroscience/news/investigational-drug-promotes-nerve-repair-in-animal-study-363644
Scientists have shown that a brain-penetrating candidate drug can foster the regeneration of damaged nerves after spinal trauma.
investigational drugnerve repairanimal studytechnologynetworks
https://www.prnewswire.com/news-releases/bayers-investigational-drug-riociguat-granted-fda-orphan-drug-designation-for-treatment-of-pulmonary-arterial-hypertension-and-chronic-thromboembolic-pulmonary-hypertension-225174802.html
/PRNewswire/ -- Bayer HealthCare today announced that the U.S. Food and Drug Administration's (FDA) Office of Orphan Products Development has granted two...
investigational drugorphan designationbayerriociguatgranted
https://www.bms.com/healthcare-providers/post-study-drug-access.html
Bristol Myers Squibb accepts requests for pre-approval access to investigational medicines from physicians for patients fighting against serious diseases.
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https://www.biospace.com/biocity-announces-fda-clearance-of-investigational-new-drug-application-for-its-first-in-class-cd3-egfr-bispecific-antibody
BioCity Biopharma announced that the U.S. Food and Drug Administration has cleared the company's Investigational New Drug application for a Phase 1 study of...
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