Ipf has a 0% survival rate without lung transplant and a median survival time of 2-5 years from diagnosis - could gri-0621 be the solution?

La jolla, ca / accesswire / september 1, 2023 / idiopathic pulmonary fibrosis (ipf) is a serious chronic lung disease characterized by the thickening and stiffening of the lung tissue surrounding the air sacs. the exact cause of ipf is unknown, but it is believed to involve a combination of genetic and environmental factors.
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