A Study of ASP1570 in Adults With Advanced Solid Tumors

  • STATUS
    Recruiting
  • End date
    May 31, 2024
  • participants needed
    138
  • sponsor
    Astellas Pharma Global Development, Inc.
Updated on 21 January 2022

Summary

This study is for adults with advanced solid tumors. Their tumor has either grown outside of the area where it started or it has spread to other parts of the body. Their cancer gets worse after standard therapy or they are unable to have standard therapy.

This study will provide more information on a potential new treatment for people with advanced solid tumors, called ASP1570.

This study will be in 2 parts.

In Part 1, the best dose of ASP1570 to give to people with advanced solid tumors will be worked out. Different small groups of people with advanced solid tumors will take lower to higher doses of ASP1570. There are 8 different doses in total, with each group staying on the same dose. After taking the lowest dose, the first group will be checked for medical problems. The next group can only take the higher dose if the first group on the lowest dose had no major medical problems. This will continue in the same way for each group. This means each group will take the next highest dose of ASP1570 as long as the previous group did not have any major medical problems.

Each group will take tablets of ASP1570 either once or twice every day in a 21-day cycle. They will continue with more treatment cycles on the same dose unless they have major medical problems, their cancer gets worse or the study doctor decides that person should stop treatment.

In Part 2, different small groups of people with advanced solid tumors will take the best dose of ASP1570 worked out from Part 1. The dose will not go above the highest dose that people took in Part 1 without getting major medical problems. Some groups of people will have specific advanced tumors. These include tumors from metastatic melanoma or non-small cell lung cancer (NSCLC for short). Other groups will have solid tumors that showed a response in Part 1. Again, each group will take tablets of ASP1570 once every day in a 21-day cycle. They will continue with more treatment cycles unless they have major medical problems, their cancer gets worse or the study doctor decides that person should stop treatment.

After treatment, people in the study will visit their clinic 45 days after their last dose of ASP1570. Then, the study clinic will contact each person in the study at least every 12 weeks until the end of the study or if they decide to leave the study.

Details
Condition Advanced Solid Tumors
Treatment ASP1570
Clinical Study IdentifierNCT05083481
SponsorAstellas Pharma Global Development, Inc.
Last Modified on21 January 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Participant has locally-advanced (unresectable) or metastatic solid tumor malignancy which is confirmed by available pathology records or current biopsy
Participant has at least 1 measurable lesion per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1. Lesions situated in a previously irradiated area are considered measurable if progression has been demonstrated in such lesions
Participant that has progressed after receiving all standard approved therapies or is no longer eligible for standard therapy
Participant has an Eastern Cooperative Oncology Group Performance Status of 0, 1, or 2\
Participant's last dose of prior antineoplastic therapy, including any immunotherapy, was at least 21 days prior to the first dose of Investigational Product(IP). A participant with epidermal growth factor receptor (EGFR) or anaplastic lymphomas kinase (ALK) mutation-positive non small cell lung cancer (NSCLC) is allowed to remain on EGFR tyrosine kinase inhibitor (TKI) or ALK inhibitor therapy until 4 days prior to the first dose of IP
Participants who have received radiotherapy must have completed this therapy (including stereotactic radiosurgery) at least 2 weeks prior to the first dose of IP
Participant's adverse events (excluding alopecia) from prior therapy have improved to grade 1 or baseline at least 14 days prior to the first dose of IP. Note: Participants with type 1 diabetes mellitus, endocrinopathies stably maintained on appropriate replacement therapy, or skin disorders (e.g., vitiligo, psoriasis, or alopecia) not requiring systemic treatment are allowed
Participant has adequate organ function prior to start of study treatment as indicated by the following laboratory values. If a participant has received a recent blood transfusion, the laboratory tests must be obtained >= 4 weeks after any blood transfusion: Absolute Neutrophil Count (ANC) >= 1500/µL; Platelets >= 100,000/µL; Hemoglobin >= 9 g/dL; Creatinine either (a) <= institutional Upper Limits of Normal (ULN) OR (b) Creatinine clearance >= 60 mL/min (calculated by Cockcroft-Gault equation); Total Bilirubin either (a) <= 1.5 x ULN or (b) Direct bilirubin <= ULN and total bilirubin < 3 x ULN (for participants with Gilbert's syndrome); aspartate aminotransferase (AST) [serum glutamic oxaloacetic transaminase (SGOT)] and alanine aminotransferase (ALT) [serum glutamic pyruvic transaminase (SGPT)] <= 2.5 x ULN without liver metastases (or <= 5 x ULN if liver metastases are present); serum potassium >= 3.4 mEq/L; serum magnesium >= 1.7 mg/dL; serum ionized calcium >= 4.7 mg/dL
Participant has activated partial thromboplastin time and international normalized ratio (INR) <= 1.5 x ULN and is not receiving anticoagulation
Female participant is not pregnant and at least one of the following conditions apply
Not a woman of childbearing potential (WOCBP)
WOCBP who agrees to follow the contraceptive guidance from the time of informed consent through at least 45 days after final IP administration
Female participant must agree not to breastfeed starting at screening and throughout
Female participant must not donate ova starting at first dose of IP and throughout the study period and for 45 days after final IP administration
the study period and for 45 days after final IP administration
Male participant with female partner(s) of childbearing potential (including breastfeeding partner) must agree to use contraception throughout the treatment period and for 45 days after final IP administration
Male participant must not donate sperm during the treatment period and for 45 days after final IP administration
Male participant with pregnant partner(s) must agree to remain abstinent or use a condom for the duration of the pregnancy throughout the study period and for 45 days after final IP administration
Participant agrees not to participate in another interventional study while receiving study treatment in the present study

Exclusion Criteria

Participant has received investigational therapy (other than an investigational EGFR TKI in a participant with EGFR activating mutations or ALK inhibitor in a participant with an ALK mutation) within 21 days or 5 half-lives, whichever is shorter, prior to the first dose of IP
Participant requires or has received systemic steroid therapy or any other immunosuppressive therapy within 14 days prior to the first dose of IP. Participants using a physiologic replacement dose of hydrocortisone or its equivalent (defined as up to 30 mg per day of hydrocortisone and up to 10 mg prednisone) are allowed
Participant has received and requires strong or moderate CYP2D6 inhibitors (e.g., bupropion, fluoxetine, paroxetine, duloxetine, abiraterone) during the study
Participant has symptomatic central nervous system (CNS) metastases or participant has evidence of unstable CNS metastases even if asymptomatic (e.g., progression on scans). Participants with previously treated CNS metastases are eligible, if they are clinically stable and have no evidence of CNS progression by imaging for at least 4 weeks prior to start of study treatment and are not requiring immunosuppressive doses of systemic steroids (> 30 mg per day of hydrocortisone or > 10 mg per day of prednisone or equivalent) for no longer than 2 weeks
Participant has an active autoimmune disease. Participants with type 1 diabetes mellitus, endocrinopathies stably maintained on appropriate replacement therapy, or skin disorders (e.g., vitiligo, psoriasis, or alopecia) not requiring systemic treatment are allowed
Participant was discontinued from prior immunomodulatory therapy due to a grade >= 3 toxicity that was mechanistically related (e.g., immune related) to the agent
Participant has a known history of human immunodeficiency virus (HIV) infection. HIV testing is not required for the purposes of this study unless mandated by local health authority
Participant has any of the following per screening serology test
Hepatitis A virus (HAV) antibodies (immunoglobulin M [IgM])
Positive hepatitis B surface antigen (HBsAg) or detectable hepatitis B DNA. Participants with negative HBsAg, positive hepatitis B core antibody (anti-HBc) and negative hepatitis B surface antibody (anti-HBs) are eligible if hepatitis B DNA is undetectable
Hepatitis C virus (HCV) antibodies unless HCV RNA is undetectable
Participant has a history of drug-induced pneumonitis (interstitial lung disease [ILD]), currently has pneumonitis or a prior history of ILD or noninfectious pneumonitis requiring high-dose glucocorticoids whether resolved or not
Participant has received a live vaccine against infectious diseases within 28 days
prior to the first dose of IP
Participant has an infection requiring systemic therapy within 14 days prior to the first dose of IP
Participant has received a prior allogenic bone marrow or solid organ transplant
Participant is expected to require another form of antineoplastic therapy while on study treatment
Participant has had a myocardial infarction or unstable angina within 6 months prior to the start of study treatment or currently has an uncontrolled illness including, but not limited to symptomatic congestive heart failure, clinically significant cardiac disease, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
Participant has inadequately controlled hypertension (defined as systolic blood pressure >150 and/or diastolic blood pressure > 100 mmHg on antihypertensive medications)
Participant has a corrected QT interval (Single ECG) using Fridericia's formula (QTcF) > 450 msec (for male and female participants) during screening. ECGs will be performed in triplicate during screening
Participant has a prior malignancy, other than the current malignancy for which the participant is seeking treatment, active (i.e., requiring treatment or intervention) within the previous 2 years except for locally curable malignancies that have been apparently cured, such as basal or squamous cell skin cancer, superficial bladder cancer or carcinoma in situ of the cervix or breast
Participant has had a major surgical procedure and has not completely recovered within 28 days prior to the first dose of IP
Participant has a history of bleeding diathesis
Participant requires use of any anticoagulation therapy
Participant has any condition which makes the participant unsuitable for study participation
Participant has a known or suspected hypersensitivity to ASP1570, or any components of the formulation used
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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