A Study to Determine the Efficacy and Safety of Luspatercept in Adult Participants and to Evaluate the Safety and Pharmacokinetics in and Adolescent Participants With Alpha (α)-Thalassemia

ConditionAnemia
Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age12+
SponsorBristol-Myers Squibb

About this trial

The purpose of the study is to evaluate the efficacy and safety of luspatercept plus best supportive care (BSC) vs placebo plus BSC on anemia in adult participants with α-thalassemia hemoglobin H (HbH) disease and determine the safety and drug levels in adolescent participants.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult participant≥ 18 years with documented diagnosis of A-Thal HbH disease with Transfusion dependence defined as:.

TD participant: ≥ 6 RBC units during the 24 weeks prior to randomization.

NTD participant:< 6 RBC units during the 24 weeks prior to randomization(transfusion due to conditions other than A-Thal will not be considered)and, RBC transfusion-free during at least 8 weeks prior to randomization(unless transfusion was required to treat an acute medical condition other than A-Thal) and, mean baseline Hb ≤ 10 g/dL, based on a minimum of 2 measurements ≥ 1 week apart within 4 weeks prior to randomization; hemoglobin values within 21 days post-transfusion will be excluded.

Adult participant has Eastern Cooperative Oncology Group (ECOG) 34 score of 0 or 1.

Disqualifiers

Medical Conditions: Diagnosis of A-ThalTrait, Hb Bart hydrops, ATRx A-Thal, hemoglobin S/β-thalassemia, myelodysplasia subtype anemia, or with HbE homozygous beta gene mutation. Anemia related to nutritional deficiency, anemia of chronic disease, autoimmune hemolytic anemia, or any other hemolytic anemias. Undergone episodes of hemolysis not related to A-Thal within the 8 weeks prior to randomization.

Participant has deep vein thrombosis (DVT), stroke or other thromboembolic event(s) (except clogged indwelling catheter) requiring medical intervention ≤ 24weeks prior to randomization.

Participant has uncontrolled hypertension. Controlled hypertension for this protocol is considered: blood pressure value corresponding to ≤Grade 1 according to NCI CTCAE Version 5.0. with or without pharmacological treatment.

Reproductive Status: Women who are pregnant, plan to get pregnant during the study, or who are breastfeeding.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Luspatercept

    Biological/Vaccine

    Specified dose on specified days

  • Placebo

    Drug

    Specified dose on specified days

Treatment groups

189 Participants
are divided into 4 treatment groups
Group A: Transfusion Dependent (TD): Luspatercept + Best supportive care (BSC)Experimental treatment 1 intervention
Group B: Adult TD Cohort: Placebo + BSCPlacebo comparator 1 intervention
Group C: Non-transfusion Dependent (NTD): Luspatercept + BSCExperimental treatment 1 intervention
Group D: Adult NTD Cohort: Placebo + BSCPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Number of participants with ≥ 50% reduction from baseline in RBC transfusion burden with a reduction of at least 2 units during any continuous 12 weeks during Week 13-48 compared to 12-week interval immediately prior to date of first dose

Adult TD Cohort

Time frame
Up to Week 48
2

Number of participants with an increase from baseline of ≥ 1.0 grams (g)/decilitre (dL) in mean hemoglobin (Hb) values over the continuous 12-week interval from Week 13 to Week 24 in the absence of RBC transfusion

Adult NTD Cohort

Time frame
Up to Week 24
3

Dose-limiting toxicities (DLTs) defined as observance of ≥ Grade 3-related hemolytic crises or ≥ Grade 3-related event outside of the known safety profile occurring within the 21 days from their first dose of study therapy

Adolescent TD and NTD Cohorts

Time frame
Up to Week 3
4

Number of participants with adverse events (AEs)

Adolescent TD and NTD Cohorts

Time frame
Up to 8.5 years

Secondary outcomes

1

Number of participants with ≥ 33% reduction from baseline in RBC transfusion burden with a reduction of at least 2 units during any continuous 24-week interval on treatment compared to 24-week interval immediately prior to date of first dose

Adult TD Cohort

Time frame
Up to Week 108
2

The longest duration with ≥ 50% reduction from baseline in RBC transfusion burden with a reduction of at least 2 units

Adult TD Cohort

Time frame
Up to Week 108
3

Number of RBC transfusion units from week 1 to week 48

Adult and Adolescent TD Cohorts

Time frame
Up to Week 48
4

Change from baseline in hemoglobin in the absence of transfusion at Week 24

Adult and Adolescent NTD Cohorts

Time frame
Up to Week 24

Other outcomes

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