LTX-315 in Patients With Transdermally Accessible Tumours as Monotherapy or Combination With Ipilimumab or Pembrolizumab

Breast Cancer Clinical Trial

Official title: A Phase I, Open-label, Multi-arm, Multi-centre, Multi-dose, Dose Escalation Study of LTX-315 as Monotherapy or in Combination With Either Ipilimumab or Pembrolizumab in Patients With Transdermally Accessible Tumours

Status Completed

Clinical Trial Summary

The study will assess the safety, tolerability, PK and efficacy of different intra-tumoral dosing regimens of LTX-315; a lytic-peptide that induces long-term anti-cancer immune responses, as monotherapy or in combination with ipilimumab or pembrolizumab.

Clinical Trial Description

In this phase I, open-label, multi-arm, multicentre, multi-dose dose escalation study in patients with transdermally accessible tumours; the safety, PK and efficacy of different dosing regimens of LTX-315 will be assessed.

Patients will be allocated into 4 separate (parallel) arms depending on the tumour type and the number of lesions available.

Arm A: Single lesion/sequential lesion treatment arm (LTX-315 monotherapy) (Completed) Arm B:

Concurrent multiple lesion treatment arm with all tumour types (LTX-315 monotherapy) Arm C:

LTX-315 combination with ipilimumab in patients with melanoma Arm D: LTX-315 combination with pembrolizumab in patients with TNBC

All patients will have at least one lesion available for injection.

Treatment schedule:

Arm A: Injection of LTX-315 3 days week 1, 1 day in week 2, 3, 4, 5 and 6. Every 2 weeks starting with week 8.

Arm B (all tumours): Injection of LTX-315 2 days week 3 weeks (Day 1, 2, 8, 9, 15 and 16).

Arm C (melanoma): Injection of lTX-315 2 days week 3 weeks (Day 1, 2, 8, 9, 15 and 16) in combination with ipilimumab given in week 1 and every 3 weeks 4 cycles.

Arm D (TNBC): Injection of LTX-315 2 days week 3 weeks (Day 1, 2, 8, 9, 15 and 16) in combination with pembrolizumab given in week 1 and every 3 weeks up to 2 years.

Patients will be enrolled into a dose cohort in order of study entry. Staring with the lowest dose. A minimum of 3 patients will be enrolled into each cohort. Dose escalation determined by the Safety Review Committee and the Sponsor. The the optimal regimen will be based on the results of the Dose Escalation from the following information:

1. Safety parameters including blood samples and cardiovascular effects

2. Immunohistology and ultrasound confirmation of necrosis and tumour infiltrating lymphocytes

3. Systemic inflammatory response

4. Evidence of clinical responses

Cohorts may be utilized to:

1. Evaluate different doses of LTX-315

2. Explore potential modifications to the dosing schedule

3. Evaluate the potential to include appropriate combination therapies with LTX-315

4. Gain further information on clinical efficacy ;

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms
• Cancer
• Head and Neck Cancer
• Head and Neck Neoplasms
• Lymphoma
• Melanoma
• Triple Negative Breast Neoplasms
• Triple-Negative Breast Cancer

• NCT number: NCT01986426
• Study type: Interventional
• Source: Lytix Biopharma AS
• Status: Completed
• Phase: Phase 1
• Start date: November 2013
• Completion date: August 31, 2018