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Individual Patient Expanded Access IND of Hope Biosciences First Blood Relative Allogeneic Adipose-derived Mesenchymal Stem Cells (HB-adMSCs) for Pancreatic Cancer

2 juli 2021 uppdaterad av: Hope Biosciences

Individual Patient Expanded Access IND of Hope Biosciences Allogeneic First Blood Relative Adipose-derived Mesenchymal Stem Cells (HB-adMSCs) for Pancreatic Cancer

The drug for this submission is Hope Biosciences' allogeneic, first blood relative, adipose-derived culture-expanded mesenchymal stem cells (HB-adMSCs) for the treatment of a single patient with Pancreatic Cancer (PC). PC is an extremely infiltrative neoplasm that usually presents with vascular and perineural invasion in surgically resected tumors. Metastases to lymph nodes, liver and distant sites are all very common. Its incidence has markedly increased over the past several decades and ranks as the fourth leading cause of cancer death in the United States. Despite the high mortality rate associated with pancreatic cancer, its etiology is poorly understood. PC patients experience physiological symptoms such as anemia, ascites, severe fatigue, pain, cachexia, weakness, insomnia, confusion, and memory loss. The aggressive nature of PC leads to rapid deterioration of patients' quality of life and diminished ability to participate in treatment.

Studieöversikt

Status

Inte längre tillgänglig

Intervention / Behandling

Detaljerad beskrivning

Once the eligibility is confirmed, approximately 1-3 weeks after the screening/baseline visit, the subject will return for the first infusion. Subsequent treatments will occur weekly for the first 8 infusions, followed by 4 infusion that occur 2 weeks apart. The total number of infusions will be 12.

On each of these visits, the subject will receive one allogeneic HB-adMSC infusion of 200 million (2 x 10^8 cells) total cells suspended in 250 mL normal saline for IV infusion. Every infusion visit will include the following procedures:

  1. Review of medical history,
  2. Complete Physical exam (Week 1, 4, 10, 20, and 52),
  3. Vital signs (Heart Rate, BP, Respirations, Temp., SpO2),
  4. Weight measurement
  5. A verification of patient consent will be verbally performed
  6. *When applicable (Week 4, 7, 10, 14, 20 and 52): A urine and blood sample for clinical labs including:

    • CBC with diff.,
    • CMP,
    • Coagulation Panel,
    • TNF-a
    • IL-6
    • CA 19-9
    • LDH
  7. The HB-adMSC infusion will be given via IV.
  8. The subject will then be monitored for a minimum of 2hr after infusion.
  9. 24-hour telephone assessment for adverse events
  10. Video Documentation

Vital signs will be continuously monitored during the infusion and recorded at 15 minutes intervals during the first hour. Vital signs will be recorded at the end of the infusion and every 30 minutes x 2 hours or more frequently if clinically indicated. The subject will be contacted by telephone 24hr. after the infusion visit to determine if any adverse events have occurred.

*Please note that blood and urine sample during the intervention period will only be required for the visits corresponding to weeks 4, 7, 10, 14, 20 and 52. During these visits, these samples will always be taken before the infusion is started. Refer to Table 1. Schedule of assessments for more details.

Follow-up Visits week 4,7, 10, 14, 20, and 52

The subject will undergo the following procedures at each follow-up visit without infusion:

  1. Review and update medical history,
  2. Update concomitant medications list
  3. Weight
  4. Vital signs (Heart Rate, BP, Respirations, Temp., SpO2),
  5. Complete physical exam (Week 1, 4, 10, 20, and 52)
  6. A urine and blood sample for clinical labs including:

    • CBC with diff.,
    • CMP,
    • Coagulation Panel,
    • TNF-a
    • IL-6
    • CA 19-9
    • LDH
  7. Adverse event monitoring.

In addition, visits 13 and 14 (week 20 and 52) will include CT Scans of the chest, abdomen and pelvis. This procedure could be done up to 7 days before or after the actual visit day, depending on availability and schedule of the imaging center. If a CT Scan has been done as standard of care within 30 days of these visits, it would meet the requirement for this assessment.

Studietyp

Utökad åtkomst

Utökad åtkomsttyp

  • Individuella patienter

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • Texas
      • Sugar Land, Texas, Förenta staterna, 77478
        • Hope Biosciences

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Barn
  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

N/A

Kön som är behöriga för studier

Manlig

Beskrivning

Inclusion Criteria:

  1. Documented diagnosis of Pancreatic Cancer
  2. Hemodynamically stable

Exclusion Criteria:

  1. Immunosuppression as defined by WBC < 3, 000 cells/ml at baseline screening.
  2. Other acute or chronic medical conditions that, in the opinion of the investigator, may increase the risks associated with study participation or HB-adMSC administration.
  3. Any abnormal, inexplicable laboratory result with no obvious cause defined.
  4. Participation in other interventional research studies. Unwillingness to return for follow-up visits

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studieregistreringsdatum

Först inskickad

10 september 2019

Först inskickad som uppfyllde QC-kriterierna

10 september 2019

Första postat (Faktisk)

12 september 2019

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

6 juli 2021

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

2 juli 2021

Senast verifierad

1 januari 2020

Mer information

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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