Trial Title:
ALG.APV-527 First-in-human Study
NCT ID:
NCT05934539
Condition:
Solid Tumor
Conditions: Keywords:
Solid Tumor
5T4
Study type:
Interventional
Study phase:
Phase 1/Phase 2
Overall status:
Recruiting
Study design:
Allocation:
N/A
Intervention model:
Sequential Assignment
Intervention model description:
Escalating ALG.APV-527 doses with a starting dose of 0.1 mg/kg and projected 6 dose
cohorts will be explored to determine the MTD and/or the RP2D. Part 1 consists of a 3 + 3
dose-escalation examination of ALG.APV-527 single agent therapy in adult patients with
RECIST Version1.1-measurable advanced solid tumors. Part 2 consists of Dose Expansion
using the RP2D, as determined during Dose Escalation.
Primary purpose:
Treatment
Masking:
None (Open Label)
Intervention:
Intervention type:
Drug
Intervention name:
ALG.APV-527
Description:
ALG.APV-527 is a human bispecific antibody in the ADAPTIR™ format with a silenced
immunoglobulin 1 (IgG1) Fc domain targeting the co-stimulatory receptor 4-1BB, expressed
on immune cells such as CD8+ T cells and natural killer (NK) cells, and the tumor
associated antigen 5T4. ALG.APV-527 is being co-developed by Alligator Bioscience AB
(Lund, Sweden) and Aptevo Therapeutics Inc. (Seattle, WA, USA) as a cancer immunotherapy.
Arm group label:
ALG.APV-527
Other name:
No other intervention names are planned for this study
Summary:
A first-in-human, multicenter, open-label, dose escalation and dose expansion phase 1
study in patients with advanced solid tumors to evaluate the safety of intravenously
administered ALG.APV-527 (Short title: ALG.APV-527 first-in-human study). Adult patients
with advanced/metastatic solid tumors likely to express 5T4 antigen who have failed
standard of care regimens for their cancer, have become refractory to standard treatment,
or for whom no effective therapy exists based on investigator judgment may be enrolled in
this study.
Part 1 (Dose Escalation): Approximately 36 evaluable patients planned to be enrolled.
Part 2 (Dose Expansion): Approximately 20 evaluable patients planned to be enrolled.
Detailed description:
This first-in-human study is an open-label, multicenter, Phase 1 study with the aim to
assess safety and tolerability and preliminary anti-tumor activity of ALG.APV-527
administered intravenously to patients with advanced solid tumor malignancies. Patients
will be required to provide tumor tissue biopsy material that has been obtained within 28
days prior to the first dose of study drug ALG.APV-527.
The trial has 2 parts, Part 1 (Dose Escalation) and Part 2 (Dose Expansion). The
Escalation Phase (Part 1) is projected to occur in 6 patient cohorts of increasing dose
levels and will explore the Maximum Tolerated Dose (MTD) and/or the RP2D. Part 1 consists
of a 3 + 3 dose-escalation examination of ALG.APV-527 single agent therapy in adult
patients with RECIST Version1.1-measurable advanced solid tumors.
The MTD is defined as the highest dose level that has 6 patients evaluable for DLT with
no more than 1 of 6 with DLT.
Part 2 (Dose Expansion):
Part 2 consists of a single agent evaluation of the safety and clinical activity of
ALG.APV-527 at its RP2D in up to 20 patients with advanced solid tumors. Part 2 will
commence after all tested dose levels have been reviewed and a RP2D has been determined.
Primary Objectives:
Primary (Dose Escalation)
- To determine the safety, tolerability, MTD of ALG.APV-527 administered intravenously
as single agent therapy
- To designate an IV dose level for the Dose Expansion Phase (RP2D) of ALG.APV-527
administered IV as single agent therapy for patients with advanced solid tumors. The
RP2D can be different from the MTD.
Primary (Dose Expansion)
• To further evaluate the safety and tolerability of ALG.APV-527 when administered
intravenously at the RP2D level as monotherapy in patients with advanced solid tumors
Criteria for eligibility:
Criteria:
Inclusion Criteria:
- Have provided signed informed consent form (ICF) for participation in the study.
- Have a diagnosis of advanced solid tumor malignancy (histologically or cytologically
documented) that is metastatic or unresectable, have received standard of care
therapy, and remaining therapeutic options are participation in a clinical study or
non-curative therapy including best supportive care.
- Have one of the following tumors: non-small cell lung cancer (NSCLC),
gastric/gastro-esophageal cancer, head and neck squamous cell carcinoma, renal cell
cancer, ovarian cancer, breast cancer, malignant pleural mesothelioma, cervical
cancer, colorectal cancer, urothelial carcinoma, endometrial cancer, pancreatic
cancer, or prostate cancer.
- Must be ≥ 18 years of age.
- ECOG performance status 0-1.
- Has provided tumor tissue biopsy material that has been obtained within 28 days
prior to the first dose of study drug with ALG.APV-527. Biopsy material may be
provided as FFPE block or as pre-cut slides of 7 to 10 sequential tissue sections.
- Should have recovered from AEs due to prior anticancer medications to at least
≤Grade 1 by CTCAE version 5.0, except for alopecia, vitiligo, resolved atopy, and
white blood cell count (see inclusion criterion #13).
- Must have at least 1 measurable lesion by computed tomography (CT) or magnetic
resonance imaging (MRI) per RECIST Version 1.1.
- Must have a life expectancy of ≥3 months.
- For women of childbearing potential and men with partners of childbearing potential,
agreement to use a highly effective method of birth control for the duration of
study treatment and for at least 9 months after the last dose of study treatment:
- Combined (estrogen and progesterone containing) hormonal contraception
associated with inhibition of ovulation (oral, intravaginal, or transdermal)
- Progestogen-only hormonal contraception associated with inhibition of ovulation
(oral, injectable, or implantable)
- Intrauterine device (IUD)
- Intrauterine hormone-releasing system (IUS)
- Bilateral tubal occlusion
- Vasectomized partner
- Sexual abstinence (defined as refraining from heterosexual intercourse during
the entire study and for 9 months after the last dose of study treatment and
must be the preferred and usual lifestyle of the patient)
- Females of childbearing potential must have a negative serum or urine pregnancy
test.
- Must have adequate coagulation function at Screening as determined by:
- PT international normalized ratio (INR) ≤ 1.5.
- PTT ≤ 1.5 × ULN. Patients on full dose of oral anticoagulation must be on this
dose for a minimum duration of 14 days before the first dose of study drug; if
receiving warfarin, the patient must have an INR ≤ 3.0 and no active bleeding
(i.e., no bleeding within 14 days prior to first dose of study drug); patients
on low molecular weight heparin will be allowed.
- Must have adequate hematologic function at Screening as determined by:
- White blood count cell (WBC) ≥ 2000/µL.
- Absolute neutrophil count (ANC) ≥ 1500/µL (patient may not use G-CSF or GMCSF
to achieve these WBC and ANC levels).
- Platelet count ≥ 100 × 103/µL.
- Hemoglobin (Hgb) ≥ 9.0 g/dL (may not transfuse or use erythropoietin to obtain
this Hgb level; transfusions are allowed up to 2 weeks prior to C1D1).
- Must have adequate renal and hepatic function at Screening as determined by:
- Adequate renal function (estimated glomerular filtration rate [eGFR] > 40
mL/min according to the Cockcroft-Gault formula).
- Total bilirubin ≤ 1.5 × ULN (or ≤ 3.0 × ULN for patients with liver metastases
or known Gilbert's syndrome).
- AST and ALT ≤ 2.5 × ULN (≤ 5.0 × ULN in patients with documented liver
metastasis).
- Alkaline phosphatase ≤ 2.5 x ULN (≤ 5.0 × ULN in patients with documented liver
or bone metastases)
- Must be able to attend study visits as required by the protocol.
Exclusion Criteria:
- Has received anti-cancer chemotherapy (including molecular-targeted drugs),
radiotherapy (therapeutic or curative intent) or hormonal therapy within 14 days
before the first dose of ALG.APV-527; however, the following are permitted:
- Hormonal therapy with gonadotropin-releasing hormone (GnRH) agonists or
antagonists for prostate cancer
- Hormone-replacement therapy or oral contraceptives
- Herbal therapy intended as anti-cancer ≥ 1 week prior to first dose of
ALG.APV-527
- Palliative radiotherapy for bone metastases within 2 weeks prior to first dose
of ALG.APV-527
- Has received immunotherapy (e.g., CAR T-cell therapy, T-cell redirecting bispecific
antibodies, mono-specific antibodies, vaccines or cytokines), or investigational
agents within 28 days before the first dose of ALG.APV-527.
- Receives concurrent systemic (oral or IV) steroid therapy >10 mg methylprednisolone
daily or its equivalent for an underlying, non-cancer condition. Concurrent
corticosteroid therapy as anticancer drug (any dose) is considered exclusionary.
- Has had major surgery within the 4 weeks before the first dose of ALG.APV-527.
- History of, or known, central nervous system (CNS) disease involvement (e.g.,
glioblastoma [GBM]), carcinomatous meningitis, CNS metastases including spinal
metastases with a risk of spinal cord compression (spinal metastases not associated
with a risk of spinal cord compression are acceptable); CNS metastases that are
treated and not progressing are acceptable.
- Has seizures requiring anticonvulsant treatment or has a history of a
cerebrovascular accident or transient ischemic attack less than 6 months ago.
- Has uncontrolled or severe intercurrent medical condition or a significant history
of renal, neurologic, psychiatric, pulmonary, endocrinologic, metabolic,
immunologic, cardiovascular, or hepatic disease that in the opinion of the
investigator would adversely affect the patient's participation in this trial.
- Has interstitial lung disease or active, non-infectious pneumonitis.
- Has a history of autoimmune disease active or past including but not limited to
inflammatory bowel disease, systemic lupus erythematosus (SLE), ankylosing
spondylitis, scleroderma, or multiple sclerosis. Has any active immunologic disorder
requiring immunosuppression with steroids >10mg methylprednisolone daily or its
equivalent or other immunosuppressive agents (e.g., azathioprine, cyclosporine A)
with the exception of patients with isolated vitiligo, resolved childhood asthma or
atopic dermatitis, controlled hypoadrenalism or hypopituitarism, and euthyroid
patients with a history of Grave's disease. Patients with controlled hyperthyroidism
must be negative for thyroglobulin, thyroid peroxidase antibodies, and
thyroid-stimulating immunoglobulin prior to study drug administration.
- Has a known hypersensitivity to a component of the protocol therapy, ALG.APV-527.
- Has a history of another primary cancer within the 5 years prior to enrollment
except for the following: non-melanoma skin cancer, cervical carcinoma in situ,
superficial bladder cancer, or other non-metastatic carcinoma that has been in
complete remission without treatment for more than 5 years.
- Has abnormal electrocardiograms (ECGs) that are clinically significant, such as QT
prolongation (corrected QT interval [QTcF] > 470 msec).
- In the opinion of the treating Investigator, has any concurrent conditions that
could pose an undue medical hazard or interfere with the interpretation of the study
results; these conditions include, but are not limited to ongoing or active
infection, clinically significant non-healing or healing wounds, concurrent
congestive heart failure (New York Heart Association Functional Classification Class
II, III or IV), concurrent unstable angina, concurrent cardiac arrhythmia requiring
treatment (excluding asymptomatic atrial fibrillation), recent (within the prior 12
months) myocardial infarction, acute coronary syndrome or stroke within the previous
12 months, significant valvular disease, cardiomegaly, ventricular hypertrophy, or
cardiomyopathy, significant pulmonary disease (shortness of breath at rest or on
mild exertion), for example, because of concurrent severe obstructive pulmonary
disease, concurrent hypertension requiring more than 2 medications for adequate
control, or diabetes mellitus with more than 2 episodes of ketoacidosis in the prior
12 months.
- Has an ejection fraction (EF) of 50% or less based on a multi-gated acquisition
(MUGA) scan or echocardiogram (ECHO).
- Patient has any active, uncontrolled, or suspected infection at the time of signing
ICF or within 3 days prior to treatment start.
- Has the presence of a known active acute or chronic infection (viral, bacterial,
systemic fungal) including human immunodeficiency virus (HIV) as determined by
enzyme-linked immunosorbent assay (ELISA) and confirmed by Western blot; and
hepatitis B virus (HBV) and hepatitis C virus (HCV) as determined by hepatitis B
surface antigen (HBsAg) and hepatitis C serology (prophylactic therapy according to
institutional protocols is acceptable).
- Has a cognitive, psychological, or psychosocial impediment that would impair the
ability of the patient to receive therapy according to the protocol or adversely
affect the ability of the patient to comply with the informed consent process,
protocol, or protocol-required visits and procedures.
- Pregnant or breastfeeding.
- Have been exposed to live attenuated vaccine within 4 weeks prior to first dose of
ALG.APV-527.
- Participation or plans to participate in another interventional clinical study while
taking part in this protocol; participation in an observational study is acceptable.
Gender:
All
Minimum age:
18 Years
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
Hematology Oncology Associates Of The Treasure Coast
Address:
City:
Port Saint Lucie
Zip:
34952
Country:
United States
Status:
Recruiting
Contact:
Last name:
Christine Gerdes
Email:
cgerdes@hemoncfl.com
Start date:
December 23, 2022
Completion date:
December 1, 2025
Lead sponsor:
Agency:
Aptevo Therapeutics
Agency class:
Industry
Collaborator:
Agency:
Alligator Bioscience AB
Agency class:
Industry
Source:
Aptevo Therapeutics
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05934539
