E.1 Medical condition or disease under investigation |
E.1.1 | Medical condition(s) being investigated |
Light chain (AL) amyloidosis involves a hematologic disorder caused by clonal plasma cells that produce misfolded immunoglobulin light chains. Overproduction of misfolded light chains results in both soluble, aggregated forms of light chains and insoluble,fibrillar deposits of abnormal AL protein (amyloid),in the tissues and organs. This can cause a range of symptoms and organ dysfunction including cardiac,renal,and hepatic dysfunction,gastrointestinal involvement and neuropathy and macroglossia |
|
E.1.1.1 | Medical condition in easily understood language |
Light chain (AL) amyloidosis is a blood disorder, which causes progressive organ damage as a result of the misfolding of proteins. This disease can produce a range of symptoms and organ dysfuction |
|
E.1.1.2 | Therapeutic area | Diseases [C] - Blood and lymphatic diseases [C15] |
MedDRA Classification |
E.1.2 Medical condition or disease under investigation |
E.1.2 | Version | 20.0 |
E.1.2 | Level | PT |
E.1.2 | Classification code | 10036673 |
E.1.2 | Term | Primary amyloidosis |
E.1.2 | System Organ Class | 10021428 - Immune system disorders |
|
E.1.3 | Condition being studied is a rare disease | Yes |
E.2 Objective of the trial |
E.2.1 | Main objective of the trial |
To evaluate the efficacy of NEOD001 plus standard of care vs. placebo plus standard of care when administered intravenously in subjects with AL amyloidosis by assessing time to all- cause mortality or cardiac hospitalization |
|
E.2.2 | Secondary objectives of the trial |
To evaluate NEOD001 plus standard of care compared to placebo plus standard of care on the following: • Change from baseline in health-related quality of life using the Short Form-36 questionnaire (SF-36v2) • Change from baseline in cardiac functional response using the 6- Minute Walk Test (6MWT) • Cardiac best response rate as assessed by N-terminal pro-brain natriuretic peptide (NT-proBNP)
Additional Secondary Objectives To evaluate NEOD001 plus standard of care compared to placebo plus standard of care in the organ-specific populations below. In addition, the safety and tolerability of NEOD001 plus standard of care will be evaluated. • Renal best response rate using established criteria in subjects with renal involvement at baseline
Please refer to Protocol section 2.3 for full list of Additional Secondary Objectives |
|
E.2.3 | Trial contains a sub-study | No |
E.3 | Principal inclusion criteria |
Subjects must meet all of the following criteria: 1. Aged ≥ 18 years 2. Newly diagnosed and AL amyloidosis treatment naïve 3. Bone marrow demonstrating clonal plasma cells 4. Confirmed diagnosis of AL amyloidosis by the following: • Histochemical diagnosis of amyloidosis determined by polarizing light microscopy of green birefringent material in Congo red-stained tissue specimens OR characteristic electron microscopy appearance AND • Confirmatory immunohistochemistry OR mass spectroscopy of AL amyloidosis 5. Confirmed diagnosis of AL amyloidosis by mass spectrometry or immunoelectron microscopy of amyloid material in tissue biopsy if the subject meets any of the following: • is black or African American • is over 75 years of age with concurrent monoclonal gammopathy OR • If the subject meets any of the above 3 conditions and has echocardiographic evidence of amyloidosis, biopsy-proven amyloidosis with a monoclonal gammopathy and no tissue is available for mass spectrometry or immunoelectron microscopy, the subject must have gene sequencing consistent with transthyretin (TTR) wild type (e.g., no TTR mutation present) AND must score 0 in technetium-99m-3,3-diphosphono-1,2 propanodicarboxylic acid (99mTc-DPD; Rapezzi 2011), hydroxymethylenediphosphonate (99mTc-HMDP; Galat 2015), or pyrophosphate (99mTc-PYP; Bokhari 2013) scintigraphy 6. Cardiac involvement as defined by all of the following: • Past documented or presently noted clinical signs and symptoms supportive of a diagnosis of heart failure in the setting of a confirmed diagnosis of AL amyloidosis in the absence of an alternative explanation for heart failure • Either an endomyocardial biopsy demonstrating AL amyloidosis or an echocardiogram demonstrating a mean left ventricular wall thickness at diastole > 12 mm in the absence of other causes (e.g., severe hypertension, aortic stenosis), which would adequately explain the degree of wall thickening • NT-proBNP ≥ 650 pg/mL and ≤ 8500 pg/mL 7. Planned first-line chemotherapy contains bortezomib administered weekly and SC 8. Adequate bone marrow reserve, hepatic function, and renal function, as demonstrated by: absolute neutrophil count (ANC) ≥ 1.0 x10^9/L • platelet count ≥ 75 x 10^9/L • hemoglobin ≥ 9 g/dL • total bilirubin ≤ 2 times the upper limit of normal (x ULN) • aspartate aminotransferase (AST) / serum glutamic oxaloacetic transaminase (SGOT) ≤ 3 x ULN • alanine aminotransferase (ALT) / serum glutamic pyruvic transaminase (SGPT) ≤ 3 x ULN • alkaline phosphatase (ALP) ≤ 5 x ULN (except for subjects with hepatomegaly and isozymes specific to liver, rather than bone) • estimated glomerular filtration rate (eGFR) ≥ 30 mL/min/1.73 m^2 as estimated by the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation 9. Seated systolic blood pressure (BP) 90-180 mmHg 10. Distance walked during each screening 6MWT is ≥30 meters and ≤550 meters 11. Women of childbearing potential (WOCBP) must have two negative pregnancy tests during Screening, the second within 24 hours prior to the first administration of study drug and must agree to use highly effective physician-approved contraception from Screening to 90 days following the last study drug administration 12. Male subjects must be surgically sterile or must agree to use highly effective physician-approved contraception from Screening to 90 days following the last study drug administration 13. Ability to understand and willingness to sign an informed consent form prior to initiation of any study procedures |
|
E.4 | Principal exclusion criteria |
Subjects must meet none of the following criteria: 1. Non-AL amyloidosis 2. NT-proBNP < 650 pg/mL or > 8,500 pg/mL 3. Meets the International Myeloma Working Group (IMWG) definition of Multiple Myeloma (see Appendix 5) *Note that subjects who meet the IMWG definition of symptomatic multiple myeloma with signs and/or symptoms attributable only to associated amyloidosis and who do not otherwise meet the criteria for diagnosis of smoldering myeloma are potentially eligible upon approval of the Sponsor. 4. Subject is eligible for and plans to undergo ASCT or organ transplant 5. Symptomatic orthostatic hypotension that in the medical judgment of the Investigator would interfere with subject’s ability to safely receive treatment or complete study assessments 6. Myocardial infarction, uncontrolled angina, severe uncontrolled ventricular arrhythmias, or ECG evidence of acute ischemia, within 6 months prior to the Month 1-Day 1 Visit 7. Severe valvular stenosis (e.g. aortic or mitral stenosis with a valve area <1.0 cm2) or severe congenital heart disease 8. ECG evidence of acute ischemia or active conduction system abnormalities with the exception of any of the following: • First degree AV-block • Second degree AV-block Type 1 (Mobitz Type 1 / Wenckebach type) • Right or left bundle branch block • Atrial fibrillation with a controlled ventricular rate (uncontrolled [i.e., >110 bpm] ventricular rate is not allowed [determined by an average of three beats in Lead II or three representative beats if Lead II is not representative of the overall ECG]) 9. Peripheral neuropathy assessed as National Cancer Institute-Common Terminology Criteria for Adverse Events ( NCI-CTCAE) Grade 2 with pain, Grade 3 or Grade 4 10. Subject is receiving oral or IV antibiotics, antifungals or antivirals within 1 week of Month 1-Day 1 with the exception of prophylactic oral agents 11. Prior treatment with hematopoietic growth factors, transfusions of blood or blood products within 1 week of Month 1-Day 1 12. Prior radiotherapy within 4 weeks of Month 1-Day 1 13. Major surgery within 4 weeks of Month 1-Day 1 or planned major surgery during the study 14. Active malignancy with the exception of any of the following: • Adequately treated basal cell carcinoma, squamous cell carcinoma, or in situ cervical cancer • Adequately treated Stage I cancer from which the subject is currently in remission and has been in remission for 2 years • Low-risk prostate cancer with Gleason score < 7 and prostate-specific antigen < 10 mg/mL • Any other cancer from which the subject has been disease-free for ≥ 2 years 15. History of severe allergy to any of the components of NEOD001 such as histidine/L histidine hydrochloride monohydrate, trehalose dehydrate, or polysorbate 20 or history of Grade ≥ 3 infusion-related AEs or hypersensitivity to another monoclonal antibody, or known hypersensitivity to diphenhydramine (or an equivalent H1 antihistamine) or acetaminophen (or its equivalent, paracetamol) 16. Known or history of uncontrolled, active human immunodeficiency virus (HIV), Hepatitis B or Hepatitis C infection 17. Prior treatment with plasma cell-directed chemotherapy, NEOD001, 11-1F4, anti-serum amyloid P antibody, doxycycline for amyloid, or other investigational treatment directed at amyloid 18. Treatment with another investigational agent within 30 days of Month 1-Day 1 19. Women who are pregnant or lactating 20. Any condition which could interfere with, or the treatment for which might interfere with, the conduct of the study or which would, in the opinion of the Investigator, unacceptably increase the subject's risk by participating in the study 21. Subject is under legal custodianship 22. History of epilepsy or seizure disorder with the exception of childhood febrile seizures 23. Waldenström's macroglobulinemia and/or immunoglobulin M (IgM) monoclonal gammopathy |
|
E.5 End points |
E.5.1 | Primary end point(s) |
Time to all-cause mortality or cardiac hospitalization |
|
E.5.1.1 | Timepoint(s) of evaluation of this end point |
As adjudicated by the CEC |
|
E.5.2 | Secondary end point(s) |
• Change from baseline to Month 9 in the Physical Component Summary (PCS) score of the SF-36v2 • Change from baseline to Month 9 in the 6MWT distance (meters) • NT-proBNP (cardiac) best response from baseline through Month 9
Additional Secondary Efficacy Endpoints
• For renal-evaluable subjects, renal best response from baseline through Month 9 • For peripheral neuropathy evaluable subjects, change from baseline to Month 9 in the NIS-LL total score • For hepatic evaluable subjects, hepatic best response from baseline to Month 9 |
|
E.5.2.1 | Timepoint(s) of evaluation of this end point |
• Change from baseline to Month 9 in the SF-36v2 • Change from baseline to Month 9 in the 6MWT distance (meters) • NT-proBNP (cardiac) best response from baseline through Month 9
• Renal best response from baseline through Month 9 • Change from baseline to Month 9 in the NIS-LL total score • Hepatic best response from baseline to Month 9 |
|
E.6 and E.7 Scope of the trial |
E.6 | Scope of the trial |
E.6.1 | Diagnosis | No |
E.6.2 | Prophylaxis | No |
E.6.3 | Therapy | Yes |
E.6.4 | Safety | Yes |
E.6.5 | Efficacy | Yes |
E.6.6 | Pharmacokinetic | Yes |
E.6.7 | Pharmacodynamic | No |
E.6.8 | Bioequivalence | No |
E.6.9 | Dose response | No |
E.6.10 | Pharmacogenetic | No |
E.6.11 | Pharmacogenomic | No |
E.6.12 | Pharmacoeconomic | No |
E.6.13 | Others | No |
E.7 | Trial type and phase |
E.7.1 | Human pharmacology (Phase I) | No |
E.7.1.1 | First administration to humans | No |
E.7.1.2 | Bioequivalence study | No |
E.7.1.3 | Other | No |
E.7.1.3.1 | Other trial type description | |
E.7.2 | Therapeutic exploratory (Phase II) | No |
E.7.3 | Therapeutic confirmatory (Phase III) | Yes |
E.7.4 | Therapeutic use (Phase IV) | No |
E.8 Design of the trial |
E.8.1 | Controlled | Yes |
E.8.1.1 | Randomised | Yes |
E.8.1.2 | Open | No |
E.8.1.3 | Single blind | No |
E.8.1.4 | Double blind | Yes |
E.8.1.5 | Parallel group | No |
E.8.1.6 | Cross over | No |
E.8.1.7 | Other | No |
E.8.2 | Comparator of controlled trial |
E.8.2.1 | Other medicinal product(s) | No |
E.8.2.2 | Placebo | Yes |
E.8.2.3 | Other | No |
E.8.2.4 | Number of treatment arms in the trial | 2 |
E.8.3 |
The trial involves single site in the Member State concerned
| No |
E.8.4 | The trial involves multiple sites in the Member State concerned | Yes |
E.8.4.1 | Number of sites anticipated in Member State concerned | 4 |
E.8.5 | The trial involves multiple Member States | Yes |
E.8.5.1 | Number of sites anticipated in the EEA | 37 |
E.8.6 Trial involving sites outside the EEA |
E.8.6.1 | Trial being conducted both within and outside the EEA | Yes |
E.8.6.2 | Trial being conducted completely outside of the EEA | No |
E.8.6.3 | If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned |
Australia |
Austria |
Belgium |
Canada |
Denmark |
France |
Germany |
Greece |
Israel |
Italy |
Netherlands |
Poland |
Spain |
United Kingdom |
United States |
|
E.8.7 | Trial has a data monitoring committee | Yes |
E.8.8 |
Definition of the end of the trial and justification where it is not the last
visit of the last subject undergoing the trial
|
The study will end when approximately 156 primary endpoint events have occurred and EOS visits have been completed for all subjects who remain on study at that time. Events are defined as deaths due to any cause, or cardiac hospitalizations as adjudicated by the CEC |
|
E.8.9 Initial estimate of the duration of the trial |
E.8.9.1 | In the Member State concerned years | 3 |
E.8.9.1 | In the Member State concerned months | 6 |
E.8.9.1 | In the Member State concerned days | 0 |
E.8.9.2 | In all countries concerned by the trial years | 3 |
E.8.9.2 | In all countries concerned by the trial months | 6 |
E.8.9.2 | In all countries concerned by the trial days | 0 |