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ClinicalTrials.gov ID

NCT07372885

Lead Sponsor

University of ManchesterOTHER

Overall Status

Not yet recruiting

Study Type

Interventional

Phase

Phase 1Phase 2

Enrollment

50Estimated

Last Update Posted

Mar 11, 2026Actual

Start Date

Feb 9, 2026Estimated

Primary Completion Date

Dec 31, 2028Estimated

Completion Date

Dec 31, 2029Estimated

Official Title

A Multi-centre Phase I/II Trial of Granulocyte-augmented Cord Blood Transplantation for Young Adults With Very Poor Risk Acute Myeloid Leukaemia.

Brief Summary

Allogeneic stem cell transplantation is the only potentially curative therapy for patients with high-risk Acute Myeloid Leukaemia, but relapse is common and remains the leading cause of death. Patients with certain mutations and those transplanted without first clearing their disease have very poor outcomes with most relapsing soon after transplant, and then surviving only a few months. A recent trial at the Royal Manchester Children's Hospital used cord blood stem cells alongside a type of white blood cell called 'granulocytes' and produced surprisingly good outcomes for children with very resistant leukaemia.

GRACE is a clinical trial for adults (<55 years) with Acute Myeloid Leukaemia that has not responded to chemotherapy or harbours mutations that predict a very poor response to conventional transplant. Participants will receive a transplant using umbilical cord blood and be given additional infusions of white blood cells, called granulocytes. The trial will be split into two parts:-The first will study the safety of this new approach. The experience of the investigators in children is that granulocyte infusions cause a fever, rash and expansion of another type of white blood cell called lymphocytes. Children that did not have this reaction did not respond to treatment. The investigators therefore believe that the reaction is necessary for the treatment to work, but the investigators must ensure that it is safe in adult patients. The trial design allows the investigators to determine the dose of granulocytes that is best tolerated and most likely to be effective.

The aim of the second part is to demonstrate that the new treatment is more effective than conventional transplantation.

The study will be conducted in three NHS transplant centres. Patients will be recruited over 36 months and followed up for a minimum of 1 year. The study is funded by Blood Cancer UK.

• Acute Myeloid Leukemia
• Stem Cell Transplantation
• Stem Cell Transplantation, Hematopoietic
• Cord Blood Stem Cell Transplantation
• Cellular Therapy

• Cord blood transplantation + conditioning + granulocytes of variable days according to study design

Ages Eligible for Study

Child (0-17)Adult (18-64)

Sexes Eligible for Study

All

Accepts Healthy Volunteers

No

Eligibility Criteria

INCLUSION CRITERIA:

1. Availability of a suitable cord blood unit

2. Age between 16 and 55 years

3. Primary diagnosis of Acute Myeloid Leukaemia (AML) or MDS/AML (as defined by ICC 2022) fitting one or more of the following criteria:

   • TP53 mutation (single- or multi-hit)
   • Presence of inv(3) (q21.3q26.2) or t(3;3)(q21.3;q26.2)
   • Adverse risk (as per ICC 2022) and >0.1% MRD by flow cytometry after 2 cycles of induction
   • AML (any risk) with partial remission (<10% blasts) after 2 cycles induction
   • Early relapse (<6 months) after chemotherapy alone (excluding t(16;16), inv(16) or t(8;21))

4. Bone marrow performed within 28 days of starting conditioning chemotherapy demonstrates either:

   • <10% blasts
   • >10% blasts with a hypocellular background (must be discussed with the trial team)

5. Suitable fitness and organ function as per the following criteria:

   • Glomerular filtration rate >50 mL/min/1.73m2
   • Ejection fraction >50%
   • FEV1 >65% without dyspnoea on mild activity
   • AST/ALT <3 x ULN
   • Bilirubin <1.5 x ULN (excluding Gilbert's syndrome)
   • Performance Status (ECOG) of 0 or 1

6. Females of and male patients of reproductive potential (i.e., not post-menopausal or surgically sterilised) must agree to use appropriate, highly effective, contraception from the point of commencing therapy until 12 months after transplant

EXCLUSION CRITERIA:

1. AML Secondary to a myeloproliferative neoplasm
2. Active CNS disease
3. Prior allogeneic stem cell transplant
4. Participation in another clinical trial that would alter any aspect of the transplant protocol or that aims to reduce the subsequent risk of relapse (discuss with trial team if unsure)
5. History of cardiac arrhythmia
6. Ischaemic heart disease, valvular heart disease or congestive cardiac failure
7. Transient ischaemic attack or cerebrovascular accident
8. Rheumatologic disease (SLE, RA, polymyositis, mixed CTD or polymyalgia rheumatica)
9. Ulcerative colitis or Crohn's disease
10. Liver cirrhosis
11. Presence of an active second malignancy
12. Uncontrolled infection, including viral reactivation (CMV, EBV)
13. HIV positive
14. Hepatitis B/C active infection with measurable viral load (patients with chronic hepatitis B or C infection require clear documentation of absence of cirrhosis by either fibroscan or biopsy, regardless of viral load)
15. Pregnancy, breastfeeding, unwilling to use contraception
16. Contraindications to administration of pooled granulocytes
17. Previous history of sensitivity to granulocytes
18. Inability of patient to give informed consent
19. Any other organ dysfunction or co-morbidity that precludes transplant in the opinion of the investigator
20. Any concern by PI

Primary Purpose

Treatment

Allocation

Randomized

Interventional Model

Sequential Assignment

Masking

None (Open Label)

Lead Sponsor

University of ManchesterOTHER

Collaborators

King's College Hospital NHS TrustOTHER

Institute of Cancer Research, United KingdomOTHER

The Christie NHS Foundation TrustOTHER

Royal Marsden NHS Foundation TrustOTHER

jake.healey@nhs.net