||||||||||JNJ-64417184 / J&J Journal: JNJ-7184, a Respiratory Syncytial Virus inhibitor targeting the connector domain of the viral polymerase. (Pubmed Central) - Jun 17, 2024 JNJ-7184 prevented RSV replication and transcription by inhibiting initiation or early elongation. JNJ-7184 was effective in air-liquid interface cultures and therapeutically in neonatal lambs, acting to drastically reverse the appearance of lung pathology.
||||||||||JNJ-64417184 / J&J Enrollment change, Trial completion date, Trial termination, Trial primary completion date: A Study to Evaluate the Effect of Renal Impairment on JNJ-64417184 and Its Two Minor Metabolites JNJ-68294291 and JNJ-65201526 in Adult Participants (clinicaltrials.gov) - Jan 14, 2021 P1, N=6, Terminated, Sponsor: Janssen Pharmaceutica N.V., Belgium JNJ-7184 was effective in air-liquid interface cultures and therapeutically in neonatal lambs, acting to drastically reverse the appearance of lung pathology. N=36 --> 6 | Trial completion date: Jul 2021 --> Nov 2020 | Recruiting --> Terminated | Trial primary completion date: Jun 2021 --> Nov 2020; company decision
||||||||||JNJ-64417184 / J&J Trial completion: A Study to Assess the Effects of Acid-Reducing Agent(s) on JNJ-64417184 in Healthy Participants (clinicaltrials.gov) - Nov 17, 2020 P1, N=14, Completed, Sponsor: Janssen Research & Development, LLC N=36 --> 6 | Trial completion date: Jul 2021 --> Nov 2020 | Recruiting --> Terminated | Trial primary completion date: Jun 2021 --> Nov 2020; company decision Recruiting --> Completed
||||||||||JNJ-64417184 / J&J Trial completion date, Trial primary completion date: A Study of JNJ-64417184, Administered as an Oral Solution, in Healthy Participants (clinicaltrials.gov) - May 27, 2020 P1, N=32, Recruiting, Sponsor: Janssen Research & Development, LLC N=32 --> 16 Trial completion date: Apr 2020 --> Aug 2020 | Trial primary completion date: Apr 2020 --> Aug 2020
||||||||||Review, Journal: Advances in respiratory virus therapeutics - A meeting report from the 6th isirv Antiviral Group conference. (Pubmed Central) - May 17, 2020 Other topics included considerations of novel endpoints such as ordinal scales and patient reported outcomes (PRO), and study design issues, and other regulatory considerations for antiviral drug development. The aim of this report is to provide a summary of the presentations given at this meeting.