Phase 1B/2 Clinical Trial Assessing the Safety, Tolerability and Preliminary Efficacy of the Intravenous Administration of Allogeneic Placental Mesenchymal Cells for the Preemptive Treatment of Patients At Risk for Acute Kidney Injury Following Cardiac Surgery (MesAKI)

Kelifarma

Status and phase: Not yet enrolling; Phase 2; Phase 1

Conditions: Preemptive Therapy of Patients At Risk for Acute Kidney Injury Following Cardiac Surgery

Treatments: Other: Vehicle (placebo); Drug: KELI-101

Study type: Interventional

Funder types: Industry

Identifiers

NCT06678399

KELI-101

Details and patient eligibility

About

This clinical trial is designed to evaluate KELI-101 versus placebo for the prevention of acute kidney disease leading to chronic kidney disease in subjects at high risk for acute kidney injury following cardiac surgery. Half of the participants will receive KELI-101, while the other half will receive a placebo.

Enrollment: 91 estimated patients

Sex: All

Ages: 45+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Pre-operative

1. Age ≥ 45 years at screening.

2. Weigh at least 50 kg and maximum 150 kg to participate in the study and must have a body mass index (BMI) below 40; BMI = Body weight (kg) / [Height (m)]2.

3. Estimated kidney volume within normal ranges (110-190 ml for male and 90-150 ml for female, ultrasound method, ellipsoid formula)

4. High risk for AKI post CABG development as assessed by investigator e.g., >9 points by Acute Renal Failure after Cardiac Surgery (Thakar Score, Cleveland Clinic Score)

5. At screening, vital signs (systolic and diastolic blood pressure and pulse rate) will be assessed in the sitting position. Sitting vital signs should be within the following ranges:

   1. oral body temperature between 35.0-37.5 °C
   2. blood pressure (systolic 100-160 mmHg, diastolic < 100 mmHg)
   3. pulse rate (50-100/min) stable with or without medication(s) as per Investigator assessment.

6. Have a pre-operative (baseline) SCr and uNGAL collected within 30 days of surgery (if multiple laboratory results are available within this time window, the most recent SCr and uNGAL values before surgery will be used to establish the baseline)

7. No known change (increase or decrease) in SCr of ≥25% and uNGAL >200% at screening visit compared to a previous value not older than 6 weeks as documented by a local laboratory using standard assay methodology.

8. Willing and able to comply with visit schedule and study procedures including post-hospitalization discharge follow-up.

9. Ability to give informed consent or have a legally acceptable representative do so for them.

   Peri-operative

10. Non-emergent cardiovascular surgery utilizing CPB with >1 hr duration time. Post-operative

11. ≥ 200% rise in uNGAL and uNGAL/Cr from baseline AND above cut-off of 34 ng/mg Cr (in nonCKD patients) within 4 hours of removal from CPB [the timeline and cut-off values TBD after Phase 1 (IA1)]

Exclusion criteria

Pre-operative

1. eGFR at screening <30 mL/min/1.73 m2 (calculated using CKD-EPI 2021 equation), or on dialysis.

2. Currently receiving renal replacement therapy.

3. Patients with bleeding risk at screening. The Investigator should make this determination in consideration of the participant's medical history and/or clinical or laboratory evidence of any of the following:

   1. History of bleeding with suspected or confirmed bleeding disorder or any other high risk for bleeding in the opinion of the investigator.
   2. Thrombocytopenia: platelet count< 100x109/L
   3. Platelet dysfunction: e.g., ADP-induced platelet aggregation lower than 60 %.
   4. Pre-existing coagulation factor deficiency: including, but not limited to, fibrinogen < 2.5-2.8 g/L

4. Any emergency surgeries performed less than 30 days before screening, including aortic dissection and/or significant congenital heart defects.

5. Class IV heart failure according to the functional classification of the New York Heart Association (NYHA).

6. Left ventricular ejection fraction < 30% (based on the last available cardiac ultrasound).

7. Scheduled to undergo cardiac surgery off CPB or with hypothermic circulatory arrest.

8. Cardiogenic shock or hemodynamic instability within four weeks before surgery, requiring inotropes or vasopressors or mechanical devices such as intra-aortic balloon counter-pulsation (IABP).

9. Have received cardiopulmonary resuscitation (CPR) within 30 days before cardiac surgery.

10. Use of other investigational drugs at the time of enrollment, or within 5 half-lives of enrollment, or until the expected pharmacodynamic (PD) effect has returned to baseline, whichever is longer; or longer if required by local regulations.

11. Patients who are post-nephrectomy

12. Uncontrolled diabetes (glycolyzed HGB <7 or another cut-off as per clinical guidelines for a particular patient)

13. Have ongoing sepsis, history of sepsis or uncontrolled infection within the past 8 weeks or untreated diagnosed infection before screening visit. Sepsis is defined as the presence of a confirmed pathogen, along with fever or hypothermia and hypoperfusion or hypotension.

14. Prescribed nephrotoxic medicines (aminoglycosides, glycopeptides, radiocontrast or other agents) within the past week, leading to increased sCr >25%

15. Recent (within the last three years) and/or recurrent history of autonomic dysfunction (e.g., recurrent episodes of fainting, palpitations, etc.).

16. Pregnant or nursing (lactating) women

17. Women of child-bearing potential are defined as all women physiologically capable of becoming pregnant unless they are using highly effective methods of contraception while taking study treatment and until the end of the study. Highly effective contraception methods include:

    1. Total abstinence (when this is in line with the preferred and usual lifestyle of the participant. Periodic abstinence (e.g., calendar, ovulation, post-ovulation methods) and withdrawal are not acceptable methods of contraception.
    2. Female bilateral tubal ligation, female sterilization (have had surgical bilateral oophorectomy with or without hysterectomy) or total hysterectomy at least six weeks before taking study treatment. In the case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow-up hormone level assessment.
    3. Male sterilization (at least 6 months before screening). For female participants in the study, the vasectomized male partner should be the sole partner for that participant.
    4. Use of oral (estrogen and progesterone), injected, or implanted hormonal methods of contraception or placement of an intrauterine device (IUD) or intrauterine system (IUS), or other forms of hormonal contraception that have comparable efficacy (failure rate < 1%), for example, hormone vaginal ring or transdermal hormone contraception Peri-, postoperative

18. Anemia and hemotransfusion.

19. History of oncological disorders.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Single Group Assignment

Masking: Quadruple Blind

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91 participants in 5 patient groups, including a placebo group

Low dose

Experimental group

Treatment:

Drug: KELI-101

High dose

Experimental group

Treatment:

Drug: KELI-101

Historical matched-control group

No Intervention group

Best dose

Experimental group

Treatment:

Drug: KELI-101

Placebo

Placebo Comparator group

Treatment:

Other: Vehicle (placebo)