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IND approval from the US FDA for theranostic SAR-Bombesin trial in prostate cancer

SYDNEY, Nov. 21, 2022 /PRNewswire/ Highlights Clarity's fifth successful Investigational New Drug (IND) application with the United States Food and Drug Administration (US FDA), opening up therapeutic applications for SAR-Bombesin A total of six products with both the diagnostic and therapeutic applications for SARTATE, SAR-bisPSMA and SAR Bombesin are now under IND for US clinical trials First therapeutic clinical program for SAR-Bombesin will be in PSMA negative metastatic castrate resistant prostate cancer, an area of high unmet need Clarity Pharmaceuticals(ASX: CU6) ("Clarity"), a clinical-stage radiopharmaceutical company with a mission to develop next-generation products that improve treatment outcomes for children and adults with cancer, announces the approval of its Investigational New Drug (IND) application by the United States Food and Drug Administration (US FDA) to evaluate its SAR-Bombesin product for identification and treatment of metastatic castrate-resi ....

United States , New South Wales , Alan Taylor , Guggerm Bombesin , Clarity Pharmaceuticals , National Cancer Institute , Technology Platform , Drug Administration , Cancer Statistics Center , American Cancer Society , Investigational New Drug , United States Food , Executive Chairman , Targeted Copper Theranostic , Gastrin Releasing Peptide , Specific Membrane Antigen Uptake , Metastatic Castration Resistant Prostate , Clin Cancer , Cancer Statistics , Mortality Worldwide , Cancer Society ,

IND approval from the US FDA for theranostic SAR-Bombesin trial in prostate cancer

SYDNEY, Nov. 21, 2022 /PRNewswire/ Highlights Clarity's fifth successful Investigational New Drug (IND) application with the United States Food and Drug Administration (US FDA), opening up therapeutic applications for SAR-Bombesin A total of six products with both the diagnostic and therapeutic applications for SARTATE, SAR-bisPSMA and SAR Bombesin are now under IND for US clinical trials First therapeutic clinical program for SAR-Bombesin will be in PSMA negative metastatic castrate resistant prostate cancer, an area of high unmet need Clarity Pharmaceuticals(ASX: CU6) ("Clarity"), a clinical-stage radiopharmaceutical company with a mission to develop next-generation products that improve treatment outcomes for children and adults with cancer, announces the approval of its Investigational New Drug (IND) application by the United States Food and Drug Administration (US FDA) to evaluate its SAR-Bombesin product for identification and treatment of metastatic castrate-resi ....

United States , New South Wales , Alan Taylor , Guggerm Bombesin , Clarity Pharmaceuticals , National Cancer Institute , Technology Platform , Drug Administration , Cancer Statistics Center , American Cancer Society , Investigational New Drug , United States Food , Executive Chairman , Targeted Copper Theranostic , Gastrin Releasing Peptide , Specific Membrane Antigen Uptake , Metastatic Castration Resistant Prostate , Clin Cancer , Cancer Statistics , Mortality Worldwide , Cancer Society ,