A PHASE Ib, OPEN-LABEL, DOSE-ESCALATION STUDY TO EVALUATE THE SAFETY AND PHARMACOKINETICS OF EFMARODOCOKIN ALFA IN COMBINATION WITH STANDARD OF CARE IN PATIENTS UNDERGOING ALLOGENEIC HEMATOPOIETIC STEM CELL TRANSPLANTATION

This is a Phase Ib, open-label, multicenter, dose-escalation study to evaluate the safety,
tolerability, and pharmacokinetics of Efmarodocokin Alfa and to make a preliminary assessment
of activity of Efmarodocokin Alfa in combination with standard-of-care (SOC) in the
prevention of acute graft-versus-host disease (aGVHD) in participants undergoing allogeneic
hematopoietic stem cell transplantation (HSCT).

Inclusion Criteria:

- Eligible for hematopoietic stem cell transplantation (HSCT)

- Donor meeting human leukocyte antigen (HLA) matching criteria of HLA-matched related
or HLA-matched unrelated (HLA-A, HLA-B, HLA-C, and HLA-DRB1, eight out of eight) from
either peripheral blood or bone marrow stem cells and meeting donor-eligibility
criteria as outlined by the U.S. Food and Drug Administration (FDA) in 21 CFR 1271
(including screening for Zika and SARS-CoV-2 exposure or infection)

- Planned HLA (HLA-A, HLA-B, HLA-C, and HLA-DRB1)-matched (eight out of eight) related
or planned HLA-matched (eight out of eight) unrelated HSCT, from either peripheral
blood or bone marrow stem cells, for patients with acute myeloid leukemia (AML) or
acute lymphocytic leukemia (ALL) in first complete remission (per institutional
criteria) or patients with intermediate or high-risk myelodysplastic syndrome (MDS)

- Planned myeloablative conditioning regimen per institutional guidelines

- Planned aGvHD prophylaxis consisting of tacrolimus and methotrexate; in cases of
tacrolimus intolerance, cyclosporine or sirolimus may be used as a substitute

Exclusion Criteria:

- Prior receipt of autologous or allogeneic HSCT

- Diagnosis of myelofibrosis or myelodysplastic/myeloproliferative overlap syndrome

- Treatment with investigational biologic or non-biologic therapy within 5 drug
elimination half-lives (or within 90 days or 30 days, respectively, if half-life is
unknown) prior to initiation of study drug

- Positive hepatitis B virus (HBV) or hepatitis C virus (HCV) serologies

- History of Grade >1 cervical intraepithelial neoplasia

- A marked baseline prolongation of QT/QTc interval

- Risk factors for torsades de pointes

- Pregnant or breastfeeding

- Any serious medical condition or abnormality in clinical laboratory tests that, in the
investigator's judgment, precludes the patient's safe participation in and completion
of the study