Dose-escalation Study of Lupartumab Amadotin (BAY1129980)

Neoplasms Clinical Trial

Official title:

An Open-label Phase I Dose-escalation Study to Evaluate the Safety, Tolerability, Maximum Tolerated Dose, Pharmacokinetics, and Pharmacodynamics of the Anti-C4.4a Antibody Drug Conjugate BAY1129980 in Subjects With Advanced Solid Tumors Known to Express C4.4a

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02134197
• Other study ID #: 16044
• Status: Terminated
• Phase: Phase 1
• Start date: May 22, 2014
• Est. completion date: August 30, 2018

Study information

• Verified date: December 2019
• Source: Bayer
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate:

• The side effects of BAY1129980 when given every 21 days different dose levels.

• Determine the dose level of BAY1129980 that should be tested in future clinical research studies.

• Measure how much BAY1129980 is in the blood at specific times after administration.

• If treatment with BAY1129980 shows any effect on reducing the tumor growth.

• If there are specific biomarkers that might be able to explain why some patients respond to treatment and others do not.

• If treatment with BAY1129980 causes an immune response from the body against the drug (immunogenicity).

Description:

The relatively restricted C4.4a expression pattern provides a target for the selective delivery of a cytotoxic drug to C4.4.a-expressing tumor cells by means of a suitable antibody-drug conjugate. The subject population eligible for the current study will be those subjects with advanced malignancies known to express C4.4a, which are refractory to standard therapy or those without standard therapy or actively refusing any treatment, which would be regarded as standard and in whom, in the opinion of the investigator, experimental therapy with BAY1129980 may be beneficial.Depending on the number of dose-escalating steps and the occurrence of DLTs, the planned numbers of subjects could vary.It is expected that up to 90 subjects may participate in the dose-expansion phase of the study and up to 6-9 subjects may particpate in the dose re-esclation phase.The study assessments in the expansion phase of the study are identical to those in the dose-escalation phase.

Amendment # 3 includes changes to DLT criteria (hematological and non-hematological) and allows for frequent follow-up for subjects experiencing drug-related liver toxicity that warrants dose reduction or dose interruptions.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 69
• Est. completion date: August 30, 2018
• Est. primary completion date: August 30, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• All subjects must be = 18 years at the first screening examination / visit

• All subjects must provide a tumor tissue sample from [Formalin Fixed Paraffin Embedded (FFPE) slides] archival tissue or fresh biopsy collected before Cycle 1, Day 1

• Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 to 1

• Life expectancy of at least 12 weeks

• Radiographically or clinically evaluable tumor. In the expansion phase, disease must be measurable according to RECIST 1.1.

• Adequate bone marrow, liver, and renal function

• Histologically or cytologically confirmed solid tumors known to express C4.4a (eg, carcinomas of the lung, head & neck SCC, esophagus SCC (squamous cell carcinoma),colon, ovary, prostate, and breast) that are refractory to any standard therapy, or have no standard therapy available, or for which subjects actively refuse any treatment that would be regarded as standard and in whom, in the opinion of the investigator, experimental therapy with BAY1129980 may be beneficial.

• A signed informed consent must be obtained prior to any study-specific procedures.

• Measurable disease with at least one lesion that can be accurately measured in at least one dimension according to RECIST 1.1

Exclusion Criteria:

• Anticancer chemotherapy, experimental cancer therapy, or cancer immunotherapy within 4 weeks prior to first dose study drug. Anticancer therapy is defined as any agent or combination of agents with clinically proven anti tumor activity administered by any route with the purpose of affecting the malignancy, either directly or indirectly, including palliative and therapeutic endpoints.

• Skin toxicity including but not limited to erythema, rash, ulceration, and open wound that is still clinically present and considered as acute or chronic.

• Subjects with psoriasis or other severe skin disease (eg, autoimmune skin disease, active erythematous skin lesions, etc.)

• Serious, non-healing wound, skin ulcer (of any grade), or bone fracture.

• Prior local radiotherapy is allowed if it is completed at least 4 weeks prior to the first dose of study drug and the subject has evaluable lesions not previously irradiated

• Significant liver dysfunction determined as Child-Pugh score B or C

• History of symptomatic metastatic brain or meningeal tumors unless the subject is >3 months from the end of definitive therapy before the first dose of study drug and has clinically or radiologically no evidence of tumor growth.

• History of clinically significant cardiac disease.

• Anti-platelet drugs within 4 weeks prior to the first dose of study drug. Anti-platelet drugs are defined as any agent or combination of agents with clinically proven anti-thrombotic activity administered by any route with the purpose of affecting blood clotting ability of the subject.

• Participation in another clinical trial in which they received active therapy within 4 weeks prior to the first dose of study drug.

• Subjects with CNS symptoms should undergo a CT scan or MRI of the brain to exclude new or progressive brain metastases. Spinal cord metastasis is acceptable. However, subjects with spinal cord compression should be excluded.

• Subjects with severe renal impairment (GFR <50 mL/min/1.73 m²) or on dialysis.

• History of organ allograft (except for corneal transplant) or autologous or allogeneic bone marrow transplant, or stem cell rescue within 3 months prior to the first dose of study drug.

• Current evidence or previous medical history of (ie, any absolute risk of latent infection) hepatitis B or C, any active hepatitis, or human immunodeficiency virus (HIV) infection. Active clinically serious infections > CTCAE Grade 2.

• Major surgery or significant trauma within 2 weeks prior to the first dose of study drug.

• Substance abuse, medical, psychological or social conditions that may interfere with the subject's participation in the study or evaluation of the study result.

• Subjects who are pregnant or are breast-feeding.

• Any condition that is unstable or could jeopardize the safety of the subject and his / her compliance to the study.

Related Conditions & MeSH terms

• Neoplasms

Intervention

Drug:
• Lupartumab Amadotin (BAY1129980)
Starting dose is 0.15mg/kg intravenous (I.V.) administration every 21 days.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Bayer

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum tolerated dose (MTD)	MTD is defined as the maximum dose at which the incidence of DLTs (dose limiting toxicities) during Cycle 1 is below 20%, or the maximum dose administered, whichever is achieved first during dose escalation.	21 days
Primary	Number of participants with adverse events as a measure of safety and tolerability		Up to 2 years
Secondary	C4.4a expression levels in tumour tissue as measured by immunohistochemistry (IHC)		Baseline
Secondary	Tumor response evaluation following RECIST 1.1 criteria		Up to 2 years
Secondary	Plasma concentration of BAY1129980 characterized by AUC (0-tlast)		2 years
Secondary	Antidrug and antibody titer		Baseline and up to 2 years

External Links

•   More information about this study, including a results summary, can be found here.