A First-in-Human Study of alpha1H in Patients With Non-muscle Invasive Bladder Cancer

Hamlet Pharma

Status and phase: Unknown; Phase 2; Phase 1

Conditions: Non-muscle Invasive Bladder Cancer

Treatments: Other: placebo; Drug: alpha1H, 74 mg/mL; Drug: alpha1H, 7.4 mg/mL; Drug: alpha1H, 37 mg/mL

Study type: Interventional

Funder types: Industry

Identifiers

NCT03560479

HP002-001

2016-004269-14 (EudraCT Number)

Details and patient eligibility

About

This study evaluates the tolerability and preliminary anti-tumour effect of alpha1H in adults with non-muscle invasive bladder cancer, who are awaiting transurethral surgery.

In the main, blinded part of the study, one group of subjects will receive treatment with alpha1H and the other half will receive placebo. In a second, dose-escalation part of the study, a third and fourth group of subjects will receive increased doses of alpha1H.

The treatment is given on 6 occasions during a period of 22 days. The study duration is 8 - 12 weeks including scheduled follow-up and up to 27 months when an optional 24-months non-interventional follow-up period is included.

Full description

Protein-lipid complexes represent a new type of tumouricidal biologicals, with broad effects against cancers of different origins. The investigational product alpha1H is a synthetic peptide, corresponding to the alpha1 domain of α-lactalbumin, in complex with oleic acid. Alpha1H is a further development product of HAMLET, a complex between human alpha-lactalbumin and oleic acid, which has shown broad anti-tumor activity with a high degree of selectivity.

This study is a combined phase 1/2, placebo controlled, double blind study in subjects with non-muscle invasive bladder cancer awaiting transurethral resection of bladder (TURB). The first, main part of the study is randomized 1/1 and the subjects will receive intravesical instillation of either alpha1H or placebo on 6 occasions during a period of 22 days (on days 1, 3, 5, 8, 15 and 22). In a second, open, dose-escalation (DE) part of the study, two additional groups will receive increased doses of alpha1H in a standard 3+3 design in order to determine a Maximum Tolerated Dose (MTD) or alternatively, a Maximum Administered Dose (MAD). The same treatment schedule as in part 1 will be followed. One group will receive a dose of 5 times the original dose and, if tolerated, the last group will receive a dose of 10 times the original dose.

Cell shedding is quantified and characterized at each treatment occasion. The bladder tumors are characterized prior treatment and prior to the scheduled surgery. Remaining tumors will be removed by TURB (according to European Association of Urology (EAU) Guidelines recommendations) and tissues will be obtained for analyses.

A follow-up Visit will take place 30 days after the last administration of study treatment.

The total study duration of the main study is 8 - 12 weeks. After the main study, the subjects may continue in an optional extended 24-months follow-up period.

Enrollment: 52 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patient with non-muscle invasive papillary bladder cancer (NMIBC) based on cystoscopy appearance, on the waiting list for TURB.
• Negative pregnancy test in women of childbearing potential.
• Appropriate methods of contraception in women of childbearing potential during study.
• Patients should be able to keep the content of the bladder for at least one hour.

Exclusion criteria

• Patient with a previous history of muscle invasive bladder cancer.
• Patient with a history of NMIBC with an interval shorter than 6 months after previous TURB.
• Previous intravesical Bacillus Calmette-Guerin (BCG) immunotherapy in the last 12 months.
• Previous intravesical chemotherapy in the last 12 months.
• Participants with any other cancer diagnosis within the last 5 years (except of skin basaliomas).
• Acute urinary tract infection
• Participants with prior radiotherapy or systemic chemotherapy.
• Participants receiving any other investigational agent or non-marketed product one month prior to Visit 1 and during the trial.
• Any concurrent illness that may render a participant ineligible or limit compliance with study requirements.
• Previously enrolled in this trial.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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52 participants in 4 patient groups, including a placebo group

alpha1H, 7.4 mg/mL

Experimental group

Description:

alpha1H (7.4 mg/mL), solution for instillation, 30 mL

Treatment:

Drug: alpha1H, 7.4 mg/mL

placebo

Placebo Comparator group

Description:

Placebo, 0.9% NaCl (sodium chloride), 30 mL

Treatment:

Other: placebo

alpha1H, 37 mg/mL

Experimental group

Description:

alpha1H (37 mg/mL), solution for instillation, 30 mL

Treatment:

Drug: alpha1H, 37 mg/mL

alpha1H, 74 mg/mL

Experimental group

Description:

alpha1H (74 mg/mL), solution for instillation, 30 mL

Treatment:

Drug: alpha1H, 74 mg/mL