$ProKidney (PROK.US)$ From April 14 Carso De-C Inmobiliaria has made a significant investment in ProKidney by purchasing 1,034,118 shares of its stock. This transaction is valued at $620,470, highlighting a strong interest and confidence in ProKidney’s potential.
TWIMO (151403908)
:
?!?!?! such a literal company name with over 200m market capitalisation grossing under 100k only??? can’t even afford a reputable doctor. this must be a joke on the investors.
$ProKidney (PROK.US)$ ProKidney Reports Third Quarter 2024 Financial Results along with Regulatory and Clinical Development Updates Following Successful FDA Type B Meeting Positive FDA confirmation that PROACT 1 Phase 3 study could be sufficient for full regulatory approval Accelerated approval pathway available with eGFR slope as surrogate endpoint Strong cash position of $406.8 million, supporting operations into 2027 Reduced R&D expenses by $0.9 million year-over-year Slight improvement...
$ProKidney (PROK.US)$ProKidney | SC 13G/A: Statement of acquisition of beneficial ownership by individuals (Amendment)-Aaron Cowen(10.47%),Suvretta Capital Management, LLC(9.8%), etc. SEC· 11 mins ago
$ProKidney (PROK.US)$Today announced that the Company will present five posters, including one late-breaking clinical trial, at the upcoming American Society of Nephrology's (ASN) Kidney Week being held on October 23-27, 2024, in San Diego, CA.
$ProKidney (PROK.US)$Reuters· 2 mins ago ProKidney Announces Strategic Updates to Its Phase 3 Program to Accelerate Rilparencel’s Registrational Path to Potential Approval in the U.S. Believes Phase 3 Regen-016 (Proact 2) Trial Is Not Required for Initial U.S. Registration
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ProKidney Stock Discussion
From April 14
Carso De-C Inmobiliaria has made a significant investment in ProKidney by purchasing 1,034,118 shares of its stock. This transaction is valued at $620,470, highlighting a strong interest and confidence in ProKidney’s potential.
ProKidney Reports Third Quarter 2024 Financial Results along with Regulatory and Clinical Development Updates Following Successful FDA Type B Meeting
Positive
FDA confirmation that PROACT 1 Phase 3 study could be sufficient for full regulatory approval
Accelerated approval pathway available with eGFR slope as surrogate endpoint
Strong cash position of $406.8 million, supporting operations into 2027
Reduced R&D expenses by $0.9 million year-over-year
Slight improvement...
SEC· 11 mins ago
ProKidney Announces Strategic Updates to Its Phase 3 Program to Accelerate Rilparencel’s Registrational Path to Potential Approval in the U.S. Believes Phase 3 Regen-016 (Proact 2) Trial Is Not Required for Initial U.S. Registration
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