RESEARCH STUDIES & Clinical Trials

Clinical Trial ID: NCT03786081 A Phase 1b/2 Open-Label Trial of Tisotumab Vedotin (HuMax®-TF-ADC) in Combination with Other Agents in Subjects with Recurrent or Stage IVB Cervical Cancer (GOG-3024)

Status

Open

Description

This is an open label, multi-center trial of tisotumab vedotin in combination with bevacizumab, pembrolizumab, or carboplatin in subjects with recurrent or stage IVB cervical cancer. The trial consists of two-parts a dose escalation part and an expansion part. The expansion part of the trial will be initiated once the Recommended Phase 2 Dose (RP2D) of the combinations have been determined in the dose escalation part.

Objective

Evaluate anti-tumor efficacy of tisotumab vedotin alone or in combination.

Treatment

Experimental: Tisotumab Vedotin + Bevacizumab Dose escalation: Tisotumab vedotin in combination with bevacizumab once every three weeks in previously treated patients Experimental: Tisotumab vedotin + Pembrolizumab Dose escalation: Tisotumab vedotin in combination with pembrolizumab once every three weeks in previously treated patients Experimental: Tisotumab vedotin + Carboplatin Dose escalation: Tisotumab vedotin in combination with carboplatin once every three weeks in previously treated patients Experimental: Tisotumab vedotin + Carboplatin Dose expansion:Tisotumab vedotin in combination with carboplatin once every three weeks in previously untreated patients Experimental: Tisotumab vedotin + Pembrolizumab Dose expansion: Tisotumab vedotin in combination with pembrolizumab once every three weeks in previously untreated patients Experimental: Tisotumab vedotin + Pembrolizumab Dose expansion: Tisotumab vedotin in combination with pembrolizumab once every three weeks in previously treate

Conditions

Cervix

Phases

I/II

Therapies

Drugs

Age Group

Adult

Main Investiagtor

Whitworth, Jenny

Practice

Gyn

Scope

National

Participating Institutions

Baptist MD Anderson Cancer Center; Baptist MD Anderson Cancer Center GOS

Eligibility

Inclusion Criteria: - Must have squamous, adenosquamous, or adenocarcinoma of the cervix and progressed on or after standard of care treatments or are ineligible or intolerant to standard of care for recurrent or stage IVB cervical cancer (Arms A, B and C only). - Must have squamous, adenosquamous, or adenocarcinoma of the cervix and must not have received prior systemic therapy for recurrent or stage IVB cervical cancer (Arms D and E only). - Must have squamous, adenosquamous, or adenocarcinoma of the cervix and progressed on or after at least one but no more than two standard of care treatments for recurrent or stage IVB cervical cancer (Arm F only). - Must have baseline measurable disease per RECIST v1.1. - Must be at least 18 years of age on the day of signing informed consent (All Arms). - Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 (All Arms). - Is not pregnant, breastfeeding, or expecting to conceive children within the projected duration of the trial and for at least 6 months after the last trial treatment administration - Women of childbearing potential must agree to use adequate contraception during and for 6 months after the last dose of trial treatment administration. - Must sign an informed consent form (ICF) indicating the trial subject understands the purpose of and procedures required for the trial and are willing to participate in the trial (All Arms). Exclusion Criteria: - Has clinically relevant bilateral hydronephrosis which cannot be alleviated by ureteral stents or percutaneous drainage. (All Arms) - Has clinical signs or symptoms of gastrointestinal obstruction and requires parenteral hydration and/or nutrition. Post-operative obstructions within 4 weeks of abdominal surgery are permitted. (All Arms) - Has clinically significant bleeding issues or risks - Prior history (within 3 months) or current evidence of hemoptysis (1/2 teaspoon or more) (Arm A only) - Recent (within 4 weeks of first dose of trial treatment) clinically significant gastrointestinal or vaginal bleeding requiring PRBC transfusion (Arm A only) - Recent (within 4 weeks of first dose of trial treatment) evidence of wound healing complications that require medical intervention (Arm A only) - Has active ocular surface disease at baseline. Subjects with prior history of cicatricial conjunctivitis are ineligible (All Arms). - Clinically significant cardiac disease - Requires anti-coagulation therapy

Nct ID Number

NCT03786081

Secondary Trial ID Number

GCT1015-05; GOG-3024

Keywords

Treatment

More Information

clinicaltrials.gov

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