Clinical Study to Assess the Safety and Preliminary Efficacy of HCR040 in Acute Respiratory Distress Syndrome

Acute Respiratory Distress Syndrome Clinical Trial

Official title:

Phase 1/2 Clinical Study to Assess the Feasibility, Safety, Tolerability and Preliminary Efficacy of the Administration of HCR040, Allogeneic Adipose-derived Adult Mesenchymal Stem Cells, in Acute Respiratory Distress Syndrome

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04289194
• Other study ID #: ALICELL-CT-01
• Secondary ID: 2019-002688-89
• Status: Completed
• Phase: Phase 1/Phase 2
• Start date: December 10, 2019
• Est. completion date: February 27, 2022

Study information

• Verified date: February 2022
• Source: Histocell, S.L.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The main objective of the study is to assess the feasibility, safety, and tolerability of the administration of HCR040, a drug whose active substance is HC016, allogeneic adipose-derived adult mesenchymal stem cells expanded and pulsed with H2O2, in patients with acute respiratory distress syndrome.

Description:

HCR040 is an investigational medicinal product whose active substance is HC016, allogeneic adipose-derived adult mesenchymal stem cells expanded and pulsed with H2O2. The main purpose of this study is to evaluate the safety and tolerability of a single administration of HCR040 using: a) two sequential escalating doses administered 96 hours post-injury to participants with moderate to severe acute respiratory distress syndrome (ARDS); and b) the determined maximum tolerated dose administered 96 hours post-injury to participants with moderate to severe ARDS. The study also includes initial exploration of efficacy. Treatment is administered by intravenous injection. The study has been divided into two phases: Phase 1 (open label): 6 participants with moderate to severe ARDS will be included in 2 sequential cohorts. Phase 2 (randomized, controlled, double-blind): 20 participants with moderate to severe ARDS will be randomly divided into two groups (control and treated).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 26
• Est. completion date: February 27, 2022
• Est. primary completion date: August 16, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Men and women = 18 years
• Patients with criteria of moderate to severe ARDS according to the Berlin Conference.
• Berlin criteria of moderate to severe ARDS given simultaneously during the 24 hours prior to entry into the study
• Patients with invasive mechanical ventilation in controlled mode (VC, PC or VCRP) adjusted to Vt=8 mL/kg, Ppl <30 cmH2O and minimum PEEP of 8 cmH2O

Exclusion Criteria:

• Participation in a previous clinical study within 28 days prior to the ARDS situation
• Administration of a previous cell therapy product in the 5 years prior to this ARDS clinical situation
• Inability to obtain Informed Consent
• Hemodynamic instability that contraindicates the intravenous cellular administration, within the defined time frame for inclusion in the study
• Alveolar hemorrhage or hemoptysis
• LTSV situation (Limitation of life support treatments)
• Major trauma in the previous 5 days
• Neoplastic processes at any time
• EPOC or severe home asthma or any other type of chronic respiratory disease requiring respiratory oxygen
• Known Child-Pugh liver disease score > B9
• Pregnant women or women of childbearing age who are not using an adequate method of contraception, or who, if they are using it, are not willing to continue using it for the duration of the trial. If the patient is menopausal or sterile, it must be documented in the medical record
• Women who are breastfeeding if unwillingly to stop at the time of recruitment
• Pulmonary transplant
• Known grade III or IV pulmonary hypertension
• States of hypercoagulability
• History of DVP or PE in the last 6 months

Related Conditions & MeSH terms

• Acute Lung Injury
• Acute Respiratory Distress Syndrome
• Respiratory Distress Syndrome
• Respiratory Distress Syndrome, Newborn
• Syndrome

Intervention

Drug:
• HCR040 (Phase 1)
(Phase 1) Intravenous administration. Open label dose escalation, 3 patients in cohort 1 (1 million cells/kg) and 3 patients in cohort 2 (2 million cells/kg)
• Placebo (Phase 2)
(Phase 2) Intravenous administration of vehicle solution
• HCR040 (Phase 2)
(Phase 2) Intravenous administration of the maximum tolerated dose (1 million cells/kg or 2 million cells/kg)

Locations

Country	Name	City	State
Spain	Hospital Universitario de Cruces	Barakaldo	Bizkaia
Spain	Fundación Jiménez Díaz	Madrid

Sponsors (1)

Lead Sponsor	Collaborator
Histocell, S.L.

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of adverse events as a measure of safety and tolerability of a single dose of HCR040 when administered by intravenous injection		One year
Secondary	Average stay in the Intensive Care Unit (ICU) 28 days after the administration of HCR040		Day 28
Secondary	Sequential Organ Failure Assessment (SOFA) index at 3, 7, 14, 21, and 28 days after the administration of HCR040	SOFA index from 0 to 4 where lower scores represent improvement	Day 28
Secondary	Mechanical ventilation-free days 28 days after the administration of HCR040		Day 28
Secondary	Percent mortality 28 days after the administration of HCR040		Day 28
Secondary	Daily pulmonary mechanics values (Ppl, DP, CRS)		One year
Secondary	Determination of lung damage using the Murray scale at day 3, 7, 14 and 28 after the administration of HCR040	Murray scale from 0 to 4 where lower scores represent improvement	Day 28
Secondary	Vasopressor-free days 28 days after the administration of HCR040		Day 28
Secondary	ICU-free days 28 days after the administration of HCR040		Day 28