Tagraxofusp-erzs, an IL-3 Diphtheria Fusion Protein, in Combination With Gemtuzumab Ozogamicin in Patients With Relapsed/Refractory AML

NCT05716009 | Active Not Recruiting Phase 1 DMC FDA Drug

• 2 other identifiers: J2287IRB00350653
• Study Type: interventional
• Target: 36
• Locations: 1 country
• Sites: 1

Brief Summary

This is an open-label Phase Ia/Ib clinical study of tagraxofusp-erzs, a novel cytokine-drug conjugate that links interleukin-3 with a truncated diphtheria toxin, in combination with gemtuzumab ozogamicin for patients with relapsed/refractory AML. The primary objective of the study is to determine the recommended phase 2 dose (RP2D) of tagraxofusp-erzs in combination with gemtuzumab ozogamicin in this patient population. Then, once RP2D is determined, to determine the safety and tolerability of combination gemtuzumab and tagraxofusp-erzs when administered at the RP2D.

Conditions

Acute Myeloid Leukemia

Keywords

AML; tagraxofusp; Stemline; CD123; Go-TAG

Outcome Measures

Primary Outcomes (2)

• Determination of the recommended phase 2 dose (RP2D) of tagraxofusp-erzs in combination with gemtuzumab ozogamicin in patient with relapsed or refractory acute myeloid leukemia (AML)

  Identification of a RP2D with a target toxicity rate of 0.2 or less based on number of adverse events defined by CTCAE v5.0 criteria

  2.5 years

• Determination of the safety and tolerability of combination gemtuzumab and tagraxofusp-erzs when administered at the RP2D.

  Assessment of RP2D safety and tolerability based on number of adverse events defined by CTCAE v5.0 criteria

  2.5 years

Secondary Outcomes (5)

• Progression free survival

  2.5 years

• Overall Survival

  2.5 years

• Overall response rate

  2.5 years

• Time to response

  2.5 years

• Duration of response

  2.5 years

Study Arms (2)

Phase 1a Dose Escalation of tagraxofusp-erzs in r/r AML

EXPERIMENTAL

Tagraxofusp-erzs and gemtuzumab ozogamicin (GO) will be administered every 4 weeks with 28 days defined as a treatment cycle. Tagraxofusp-erzs dose escalation for cycles 1-4 in combination with fixed dose GO. This is a dose escalation design . The dose-limiting toxicity (DLT) period will be the 28 days following the first dose of GO. The initial dose level 1 (DL1) cohort will receive GO 3mg/m2 (capped at a maximum dose of 4.5mg) intravenously (IV) on cycle 1 days 1, 4, and 7 and tagraxofusp-erzs at an initial dose of 7μg/kg/day on days 10, 11, 12. For subsequent cycles of DL1, GO will continue to be administered at a dose of 3mg/m2 IV on day 1 and tagraxofusp-erzs will be administered IV at a dose of 7μg/kg/day on days 4,5,and 6. Subsequent escalation dose levels will receive tagraxofusp-erzs doses of 7mcg/kg/day, 9mcg/kg/day or 12mcg/kg/day. Initial cycle doses of tagraxofusp at these levels will be given on Days 5,6 and 7, then in subsequent cycles on days 1,2 and 3.

Drug: Dose Escalation -tagraxofusp-erzs

Phase 1b recommended Phase 2 dose (RP2D) of tagraxofusp- erzs in r/r AML

EXPERIMENTAL

This is dose expansion at the RP2D of tagraxofusp. Participants with relapsed or refractory acute myeloid leukemia (r/r AML) will receive the RP2D of tagraxofusp-erzs, as determined in Phase 1a, and gemtuzumab at a dose of 3mg/m2 (max absolute dose of 4.5mg) on days 1,4, and 7 of cycle 1 and day 1 of subsequent cycles.

Drug: Dose Expansion at RP2D -tagraxofusp-erzs

Interventions

Dose Escalation -tagraxofusp-erzs DRUG

Sequential dose levels of tagraxofusp-erzs dependent on patient response. Fixed doses of gemtuzumab ozogamicin 3mg/m2/day on days 1, 4, and 7 of cycle 1 then on Day 1 or all subsequent cycles for a total of 3 cycles.

Also known as: gemtuzumab ozogamicin

Phase 1a Dose Escalation of tagraxofusp-erzs in r/r AML

Dose Expansion at RP2D -tagraxofusp-erzs DRUG

Following the dose escalation portion, the expansion dose and schedule (RP2D) will be determined. Patients will continue to receive fixed doses of gemtuzumab ozogamicin 3mg/m2/day on days 1, 4, and 7 of cycle 1 then on Day 1 or all subsequent cycles for a total of 3 cycles.

Also known as: gemtuzumab ozogamicin

Phase 1b recommended Phase 2 dose (RP2D) of tagraxofusp- erzs in r/r AML

Eligibility Criteria

• Age: 12 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

• Histologically confirmed diagnosis of acute myeloid leukemia (AML) according per 2016 World Health Organization (WHO) criteria.
• Cluster of differentiation marker (CD)33 and CD123 / interleukin (IL)3RA expression on the subject's blasts, determined by standard Flow AML MRD assay.
• Age ≥ 12
• Relapsed or refractory after one cycle of prior therapy (cytoreductive agents such as hydroxyurea, cyclophosphamide, or a single dose of gemtuzumab ozogamicin are not considered prior treatment regimens).
• Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0, 1, or 2
• Adequate baseline organ function, including cardiac, renal, and hepatic function as defined by:
• Left ventricular ejection fraction (LVEF) ≥ 50% by multi-gated acquisition scan (MUGA) or 2-dimensional (2-D) echocardiogram (ECHO) within 28 days prior to the start of therapy
• No clinically significant abnormalities on a 12-lead electrocardiogram (ECG)
• Creatinine Clearance (CrCl) ≥ 60mL/min
• Serum albumin ≥ 3.2 g/dL (note that albumin infusions are not permitted in order to enable eligibility)
• Total bilirubin ≤ 1.5 mg/dL
• Aspartate transaminase (AST) and alanine transaminase (ALT) ≤ 2.5 times the upper limit of normal (ULN)
• white blood cell (WBC) \< 20,000/uL on day of first therapy, cytoreduction may be achieved using hydroxyurea.
• Ability to understand and willingness to sign a written informed consent document.
• Able to adhere to study visit schedule and other protocol requirements including follow up for survival assessment.

You may not qualify if:

• Prior treatment with tagraxofusp-erzs.
• Primary resistance to or progression on gemtuzumab. Patients who have previously received Gemtuzumab, but whose disease was not resistant or did not progress on it are eligible.
• Active central nervous system involvement. Patients with a history of central nervous system involvement that has cleared with prior treatments are eligible.
• Blood or bone marrow transplant within 60 days of screening or active graft versus host disease.
• The patient has persistent clinically significant toxicities Grade ≥ 2 from previous therapies, including cytotoxic chemotherapy, targeted therapies, biological therapies, or immunotherapies, not readily controlled by supportive measures (excluding alopecia, nausea, and fatigue)
• The patient has received treatment with chemotherapy, wide-field radiation, or biologic therapy within 14 days of study entry.
• The patient has an active malignancy and/or cancer history that may confound the assessment of the study endpoints. Patients with a past cancer history (within 2 years of entry) with substantial potential for recurrence and/or ongoing active malignancy must be discussed with the Sponsor before study entry. Patients with the following neoplastic diagnoses are eligible: non-melanoma skin cancer, carcinoma in situ, cervical intraepithelial neoplasia, organ-confined prostate cancer with no evidence of progressive disease.
• The patient has clinically significant cardiovascular disease (e.g. uncontrolled or any New York Heart Association Class 3 or 4 congestive heart failure, uncontrolled angina, history of myocardial infarction, unstable angina or stroke within 6 months prior to study entry, uncontrolled hypertension or clinically significant arrhythmias not controlled by medication).
• The patient has uncontrolled, clinically significant pulmonary disease (e.g. chronic obstructive pulmonary disease, pulmonary hypertension) that in the opinion of the Investigator would put the patient at significant risk for pulmonary complications during the study.
• The patient is receiving immunosuppressive therapy - with the exception of low-dose prednisone (≤10 mg/day) - for treatment or prophylaxis of graft-versus-host disease (GVHD). If the patient has been on immunosuppressive treatment or prophylaxis for GVHD, the treatment(s) must have been discontinued at least 14 days prior to study treatment and there must be no evidence of Grade ≥ 2 GVHD.
• The patient has uncontrolled intercurrent illness including, but not limited to, uncontrolled infection, disseminated intravascular coagulation, or psychiatric illness/social situations that would limit compliance with study requirements.
• The patient is pregnant or breastfeeding.
• The patient has a history of human immunodeficiency virus (HIV) infection, active or chronic Hepatitis B, or Hepatitis C.
• The patient has any condition which, in the opinion of the Investigator, places the patient at an unacceptably high risk for toxicities.

Sponsors & Collaborators

• Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins: lead
• StemlineTherapeutics, Inc.: collaborator

Study Sites (1)

The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

Baltimore, Maryland, 21287, United States

Location

MeSH Terms

Conditions

Leukemia, Myeloid, Acute

Interventions

Gemtuzumab

Condition Hierarchy (Ancestors)

Leukemia, Myeloid; Leukemia; Neoplasms by Histologic Type; Neoplasms; Hematologic Diseases; Hemic and Lymphatic Diseases

Intervention Hierarchy (Ancestors)

Calicheamicins; Aminoglycosides; Glycosides; Carbohydrates; Antibodies, Monoclonal, Humanized; Antibodies, Monoclonal; Antibodies; Immunoglobulins; Immunoproteins; Blood Proteins; Proteins; Amino Acids, Peptides, and Proteins; Serum Globulins; Globulins

Study Officials

• Alexander Ambinder, MD

  SKCCC Johns Hopkins Medical Institution

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SEQUENTIAL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Model Details: Tagraxofusp-erzs dose escalation study combined with a fixed dose of gemtuzumab ozogamicin 3mg/m2/day on days 1, 4, and 7. Dose level 1, cycle 1 of tagraxofusp-erzs will be 7mcg/kg/day on days 10, 11 and 12. Subsequent cycles at dose level 1 will consist of gemtuzumab ozogamicin 3mg/m2/day on day 1 and tagraxofusp-erzs 7mcg/kg/day on days 4, 5, and 6. For dose levels 2 through 4, gemtuzumab will continue to be administered at a fixed dose of 3mg/m2/day on days 1, 4, and 7 while tagraxofusp-erzs will be administered at escalating doses of 9mcg/kg/day then 12mcg/kg/day on days 5, 6, and 7 of cycle 1 and days 1, 2, and 3 of subsequent cycles.

Study Record Dates

• First Submitted: January 27, 2023
• First Posted: February 8, 2023
• Study Start: November 20, 2023
• Primary Completion (Estimated): December 25, 2027
• Study Completion (Estimated): December 25, 2028
• Last Updated: May 6, 2025

Record last verified: 2025-05

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)