First-in-Human Study of XMT-1592 in Patients With Ovarian Cancer and NSCLC Likely to Express NaPi2b

STATUS

Recruiting
participants needed

120
sponsor

Mersana Therapeutics

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Updated on 19 February 2024

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cancer

measurable disease

metastasis

solid tumour

lung cancer

fallopian tube

ovarian cancer

primary peritoneal carcinoma

peritoneal cancer

alopecia

hormonal contraception

hair thinning

non-small cell lung cancer

Summary

Phase 1b, a study in high grade serous ovarian cancer and nonsmall cell lung cancer to evaluate the safety and clinical activity of the antibody-drug conjugate (ADC) XMT-1592.

Description

This Phase 1b trial is an open-label, multi-center study of XMT-1592 administered as an intravenous infusion once every 3 weeks. The dose-escalation (DES) segment of the study will establish the expansion (EXP) dose and is intended to establish the maximum tolerated dose (MTD) or recommended Phase 2 dose (RP2D) for XMT-1592 in patients with high grade serous ovarian cancer (HGSOC) or non-small cell lung cancer (NSCLC), adenocarcinoma subtype. The EXP segment of the study will consist of 2 parallel cohorts of patients (HGSOC and NSCLC) to confirm the MTD or RP2D and estimate the objective response rate in each selected patient population. In DES, the observation period for dose-limiting toxicities is 21 days, between Day 1 through the end of Cycle 1 which includes the pre-dose assessments before receiving the Cycle 2 dose. All adverse events (AEs) will be graded according to NCI, CTCAE v5.0). In general, AEs Grade 3 are dose-limiting toxicities with some modifications.

Details

Condition	Non-Small Cell Lung Cancer, Non-Small Cell Lung Cancer, Ovarian disorder, Ovarian Cancer, Ovarian Cancer
Age	18years - 95years
Treatment	XMT-1592
Clinical Study Identifier	NCT04396340
Sponsor	Mersana Therapeutics
Last Modified on	19 February 2024

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Eligibility		Yes	No	Not Sure
Inclusion Criteria
	Ability to give informed consent
	ECOG performance status 0 or 1
	Measurable disease as per RECIST, version 1.1. Resolution of all acute toxic effects of prior therapy or surgical procedures to Grade 1 (except alopecia)
	Adequate organ function
	Confirmed availability of tumor tissue blocks or freshly cut tissue slides for NaPi2b testing. -In EXP, ability to undergo a fresh biopsy before enrollment, unless not medically feasible
	For women of childbearing potential and men with partners of childbearing potential, agreement to use a highly effective form of hormonal contraception or two effective forms of non-hormonal contraception by the patient and/or partner, and to continue the use of contraception for the duration of study treatment and for at least 6 months after the last dose of study treatment
	Histologically or cytologically confirmed solid tumors of the types specified below, with incurable, locally advanced or metastatic disease that has failed standard therapy or for which no standard treatment option exists
	Ovarian Cancer: Histological diagnosis of epithelial ovarian, fallopian tube, or primary peritoneal cancer, excluding the mucinous subtype
	NSCLC: Histological diagnosis of nonsquamous NSCLC
Exclusion Criteria
	Major surgery within 28 days of starting study treatment; -or- systemic anti-cancer therapy within the lesser of 28 days or 5 half-lives of the prior therapy before starting study treatment -or- recent radiation therapy with unresolved toxicity
	Brain metastases that are: untreated, progressive, have required any type of major treatment, e.g., whole-brain radiation treatment, adjuvant chemotherapy, gamma knife, to control symptoms from brain metastases within 30 days of the first study treatment. Or any history of leptomeningeal metastasis
	Current known active infection with HIV, hepatitis B virus, or hepatitis C virus
	No prior history of liver disease such as liver cirrhosis, hepatic fibrosis
	Current severe, uncontrolled systemic disease (e.g., clinically significant cardiovascular, pulmonary, or metabolic disease) or intercurrent illness that could interfere with per-protocol evaluations
	Severe dyspnea at rest due to complications of advanced malignancy, or requiring supplementary oxygen therapy
	Currently active pneumonitis or interstitial lung disease
	Pregnant or nursing women
	History of other malignancy within the last 5 years, except for appropriately treated carcinoma in situ of the cervix, non-melanoma skin carcinoma, or other malignancy with a similar expected curative outcome
	Participation in the DES component of the study
	Prior use of mirvetuximab soravtansine or another ADC containing an auristatin or maytansinoid payload

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First-in-Human Study of XMT-1592 in Patients With Ovarian Cancer and NSCLC Likely to Express NaPi2b