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ProKidney Corp., a clinical-stage biotechnology, engages in developing cellular therapy candidates. It is developing Renal Autologous Cell Therapy, an autologous homologous cell admixture that is in a Phase III development program, as well as Phase II clinical trials for the treatment of moderate to severe diabetic kidney disease; and Phase I clinical trial for patients with congenital anomalies of the kidney and urinary tract. The company was founded in 2015 and is headquartered in Winston-Salem, North Carolina.

ProKidney Corp.

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WINSTON-SALEM, N.C., NOV. 10, 2025 (GLOBE NEWSWIRE) -- PROKIDNEY CORP. (NASDAQ: PROK)(PROKIDNEY OR THE COMPANY"), A LEADING LATE CLINICAL-STAGE CELL THERAPY COMPANY FOCUSED ON CHRONIC KIDNEY DISEASE (CKD), TODAY REPORTED FINANCIAL RESULTS FOR THE THIRD QUARTER ENDED SEPTEMBER 30, 2025, AND PROVIDED REGULATORY AND CLINICAL UPDATES.

PROKIDNEY REPORTS THIRD QUARTER 2025 FINANCIAL RESULTS AND PROVIDES REGULATORY AND CLINICAL UPDATES

WINSTON-SALEM, N.C., NOV. 06, 2025 (GLOBE NEWSWIRE) -- PROKIDNEY CORP. (NASDAQ: PROK)(PROKIDNEY OR THE COMPANY"), A LEADING LATE CLINICAL-STAGE CELL THERAPY COMPANY FOCUSED ON CKD, TODAY PRESENTED FULL RESULTS FROM THE PHASE 2 REGEN-007 TRIAL EVALUATING RILPARENCEL IN PATIENTS WITH ADVANCED CKD AND DIABETES. THE DATA, FEATURED IN A LATE-BREAKING CLINICAL TRIALS PRESENTATION AT THE AMERICAN SOCIETY OF NEPHROLOGY (ASN) KIDNEY WEEK 2025, FURTHER DEMONSTRATE THE POTENTIAL OF RILPARENCEL TO PRESERVE KIDNEY FUNCTION IN PATIENTS WITH ADVANCED CKD AND DIABETES WHO ARE AT HIGH RISK OF KIDNEY FAILURE AND HAVE LIMITED THERAPEUTIC OPTIONS.

PROKIDNEY PRESENTS FULL RESULTS FROM THE PHASE 2 REGEN-007 TRIAL OF RILPARENCEL AT THE AMERICAN SOCIETY OF NEPHROLOGY KIDNEY WEEK 2025

WINSTON-SALEM, N.C., OCT. 29, 2025 (GLOBE NEWSWIRE) -- PROKIDNEY CORP. (NASDAQ: PROK)(PROKIDNEY OR THE COMPANY"), A LEADING LATE CLINICAL-STAGE CELLULAR THERAPEUTICS COMPANY FOCUSED ON CHRONIC KIDNEY DISEASE (CKD), TODAY ANNOUNCED THAT SENIOR MEMBERS OF THE MANAGEMENT TEAM WILL BE PARTICIPATING IN THE FOLLOWING TWO UPCOMING HEALTHCARE CONFERENCES IN NOVEMBER:

PROKIDNEY TO PARTICIPATE IN TWO UPCOMING CONFERENCES: GUGGENHEIM HEALTHCARE INNOVATION CONFERENCE AND THE JEFFERIES GLOBAL HEALTHCARE CONFERENCE

WINSTON-SALEM, N.C., OCT. 20, 2025 (GLOBE NEWSWIRE) -- PROKIDNEY CORP. (NASDAQ: PROK)(PROKIDNEY OR THE COMPANY"), A LEADING LATE CLINICAL-STAGE CELLULAR THERAPEUTICS COMPANY FOCUSED ON CHRONIC KIDNEY DISEASE (CKD), TODAY ANNOUNCED THAT THE COMPANY WILL PRESENT TWO POSTERS, INCLUDING A LATE-BREAKING POSTER ON THE PHASE 2 REGEN-007 STUDY RESULTS, AT THE UPCOMING AMERICAN SOCIETY OF NEPHROLOGY'S (ASN) KIDNEY WEEK BEING HELD FROM NOVEMBER 6-9, 2025, IN HOUSTON, TX.

PROKIDNEY ANNOUNCES TWO ABSTRACTS SELECTED FOR PRESENTATION AT THE AMERICAN SOCIETY OF NEPHROLOGY'S KIDNEY WEEK 2025

WINSTON-SALEM, N.C., AUG. 12, 2025 (GLOBE NEWSWIRE) -- PROKIDNEY CORP. (NASDAQ: PROK) (PROKIDNEY OR THE COMPANY"), A LEADING LATE CLINICAL-STAGE CELL THERAPEUTICS COMPANY FOCUSED ON CHRONIC KIDNEY DISEASE (CKD), TODAY REPORTED FINANCIAL RESULTS FOR THE SECOND QUARTER ENDED JUNE 30, 2025, AND PROVIDED REGULATORY AND CLINICAL UPDATES.

PROKIDNEY REPORTS SECOND QUARTER 2025 FINANCIAL RESULTS AND PROVIDES REGULATORY AND CLINICAL UPDATES

WINSTON-SALEM, N.C., JULY 15, 2025 (GLOBE NEWSWIRE) -- PROKIDNEY CORP. (NASDAQ: PROK) (PROKIDNEY OR THE COMPANY"), A LEADING LATE CLINICAL-STAGE CELLULAR THERAPEUTICS COMPANY FOCUSED ON CHRONIC KIDNEY DISEASE (CKD), TODAY ANNOUNCED CONFIRMATION OF ALIGNMENT WITH THE U.S. FOOD AND DRUG ADMINISTRATION (FDA) ON THE ACCELERATED APPROVAL PATHWAY FOR RILPARENCEL. RILPARENCEL IS AN AUTOLOGOUS CELLULAR THERAPY THAT RECEIVED REGENERATIVE MEDICINE ADVANCED THERAPY (RMAT) DESIGNATION FROM THE FDA AND CURRENTLY IS BEING EVALUATED IN THE ONGOING PHASE 3 REGEN-006 (PROACT 1) TRIAL TO DEMONSTRATE THE THERAPY'S POTENTIAL TO PRESERVE KIDNEY FUNCTION IN PATIENTS WITH ADVANCED CKD AND TYPE 2 DIABETES.

PROKIDNEY ANNOUNCES ALIGNMENT WITH THE FDA ON THE ACCELERATED APPROVAL PATHWAY FOR RILPARENCEL

WINSTON-SALEM, N.C., JULY 09, 2025 (GLOBE NEWSWIRE) -- PROKIDNEY CORP. (NASDAQ: PROK) (PROKIDNEY OR THE COMPANY), A LEADING LATE CLINICAL-STAGE CELLULAR THERAPEUTICS COMPANY FOCUSED ON CHRONIC KIDNEY DISEASE (CKD), TODAY ANNOUNCED THAT SENIOR MEMBERS OF THE MANAGEMENT TEAM WILL BE PARTICIPATING IN THE UPCOMING H.C. WAINWRIGHT 4TH ANNUAL KIDNEY VIRTUAL CONFERENCE:

PROKIDNEY TO PARTICIPATE IN THE H.C. WAINWRIGHT 4TH ANNUAL KIDNEY VIRTUAL CONFERENCE

WINSTON-SALEM, N.C., JULY 08, 2025 (GLOBE NEWSWIRE) -- PROKIDNEY CORP. (NASDAQ: PROK) (PROKIDNEY OR THE COMPANY"), A LEADING LATE CLINICAL-STAGE CELLULAR THERAPEUTICS COMPANY FOCUSED ON CHRONIC KIDNEY DISEASE (CKD), TODAY REPORTED STATISTICALLY SIGNIFICANT AND CLINICALLY MEANINGFUL POSITIVE TOPLINE RESULTS FROM THE FULL GROUP 1 MODIFIED INTENT-TO-TREAT (MITT) POPULATION OF THE PHASE 2 REGEN-007 TRIAL EVALUATING RILPARENCEL IN PATIENTS WITH CKD AND DIABETES. RILPARENCEL IS AN AUTOLOGOUS CELLULAR THERAPY THAT HAS RECEIVED REGENERATIVE MEDICINE ADVANCED THERAPY (RMAT) DESIGNATION FROM THE U.S. FOOD & DRUG ADMINISTRATION (FDA) AND IS CURRENTLY BEING EVALUATED IN THE ONGOING PHASE 3 REGEN-006 (PROACT 1) TRIAL TO DEMONSTRATE THE THERAPY'S POTENTIAL TO PRESERVE KIDNEY FUNCTION IN PATIENTS WITH ADVANCED CKD AND TYPE 2 DIABETES.

PROKIDNEY REPORTS STATISTICALLY AND CLINICALLY SIGNIFICANT TOPLINE RESULTS FOR THE PHASE 2 REGEN-007 TRIAL EVALUATING RILPARENCEL IN PATIENTS WITH CHRONIC KIDNEY DISEASE AND DIABETES

WINSTON-SALEM, N.C., JULY 01, 2025 (GLOBE NEWSWIRE) -- PROKIDNEY CORP. (NASDAQ: PROK) (PROKIDNEY OR THE COMPANY"), A LEADING LATE CLINICAL-STAGE CELLULAR THERAPEUTICS COMPANY FOCUSED ON CHRONIC KIDNEY DISEASE (CKD), TODAY ANNOUNCED THE COMPLETION OF THE DOMESTICATION PROCESS TO CHANGE THE JURISDICTION OF INCORPORATION OF THE COMPANY FROM THE CAYMAN ISLANDS TO DELAWARE. THE DOMESTICATION WAS APPROVED BY SHAREHOLDERS OF THE COMPANY AT ITS ANNUAL GENERAL MEETING HELD ON MAY 29, 2025. EFFECTIVE AS OF JULY 1, 2025, EACH (I) CLASS A ORDINARY SHARE AUTOMATICALLY CONVERTED INTO ONE SHARE OF CLASS A COMMON STOCK OF PROKIDNEY CORP., A DELAWARE CORPORATION AND (II) EACH CLASS B ORDINARY SHARE AUTOMATICALLY CONVERTED INTO ONE SHARE OF CLASS B COMMON STOCK OF PROKIDNEY. PROKIDNEY COMMON STOCK WILL BEGIN TRADING ON JULY 2, 2025, AND THE COMPANY'S TRADING SYMBOL ON THE NASDAQ STOCK MARKET WILL REMAIN UNCHANGED AS "PROK." THE COMPANY'S CUSIP NUMBER RELATING TO ITS CLASS A COMMON STOCK CHANGED TO 74291D 104. THE COMPANY DOES NOT ANTICIPATE ANY IMPACT TO DAY-TO-DAY BUSINESS OPERATIONS AS A RESULT OF THE DOMESTICATION.

PROKIDNEY CORP. COMPLETES DOMESTICATION FROM THE CAYMAN ISLANDS TO DELAWARE

WINSTON-SALEM, N.C., MAY 12, 2025 (GLOBE NEWSWIRE) -- PROKIDNEY CORP. (NASDAQ: PROK) (PROKIDNEY OR THE COMPANY"), A LEADING LATE CLINICAL-STAGE CELLULAR THERAPEUTICS COMPANY FOCUSED ON CHRONIC KIDNEY DISEASE (CKD), TODAY REPORTED FINANCIAL RESULTS AND BUSINESS HIGHLIGHTS FOR THE FIRST QUARTER ENDED MARCH 31, 2025.

ProKidney Corp.

PROK

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ProKidney Corp.

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PROK