A Study to Assess Adverse Events, Change in Disease Activity and How Intravenous (IV) ABBV901 Moves Through the Body Alone or in Combination With Other Anticancer Drugs in Adult Participants With Ovarian Cancer

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18+
SponsorAbbVie

About this trial

Ovarian cancer (OC) is a lethal disease. The purpose of this study is to assess the safety, pharmacokinetics and efficacy of ABBV901, alone or in combination with other anticancer drugs, in participants with ovarian cancer.

ABBV901 is an investigational drug for the treatment of ovarian cancer. This study has 6 parts where participants will receive ABBV-901, alone or in combination with other anticancer therapies. Around 285 participants will be enrolled in the study at approximately 45 sites around the world.

In part 1, participants will receive escalating doses of intravenous (IV) ABBV-901 alone. In part 2, participants will receive 1 of 3 doses of IV ABBV-901 alone to determine the optimized dose. In part 3, participants will receive escalating doses of IV ABBV-901 in combination with IV bevacizumab. In part 4, participants will receive recommended doses for expansion of IV ABBV-901 combination with IV bevacizumab. in Part 5, participants will receive escalating doses of IV ABBV-901 in combination with IV carboplatin and IV bevacizumab and in part 6, participants will receive recommended doses for expansion of IV ABBV-901 combination with IV carboplatin and IV bevacizumab. The total study duration will be approximately 3 years.

There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic and may require frequent medical assessments, blood tests, and scans.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosis of an advanced or unresectable malignant high grade serous epithelial ovarian, fallopian tube, and primary peritoneal cancers (EOC), fallopian tube or primary peritoneal cancer by histology (World Health Organization [WHO] criteria).

Participants enrolled in backfill (Part 1) must provide consent to paired fresh biopsies which are pretreatment and on-treatment tumor biopsies from the same tumor lesion.

Disqualifiers

Ovarian Cancer (OC) with histologies other than high grade serous OC including endometrioid, low grade, mucinous, carcinosarcoma or sarcomatous histology, mixed tumors or low grade/borderline ovarian tumor.

Participants with platinum refractory disease.

Prior therapy with an antibody-drug conjugate containing a topoisomerase inhibitor.

Prior history of Grade >= 2 interstitial lung disease (ILD) or pneumonitis.

Trial design

Design model

Sequential

Treatments tested in this trial

  • ABBV-901

    Drug

    Intravenous (IV)

  • Bevacizumab

    Drug

    Intravenous (IV)

  • Carboplatin

    Drug

    Intravenous (IV)

Treatment groups

285 Participants
are divided into 8 treatment groups

8

Treatment groups

See each treatment group below.

Group A: Part 1: ABBV-901 Dose EscalationExperimental treatment 1 intervention
Group B: Part 2: ABBV-901 Optimization Dose AExperimental treatment 1 intervention
Group C: Part 2: ABBV-901 Optimization Dose BExperimental treatment 1 intervention
Group D: Part 2: ABBV-901 Optimization Dose CExperimental treatment 1 intervention
Group E: Part 3: ABBV-901 + Bevacizumab EscalationExperimental treatment 2 interventions
Group F: Part 4: ABBV-901 + Bevacizumab ExpansionExperimental treatment 2 interventions
Group G: Part 5: ABBV-901 + Carboplatin + Bevacizumab EscalationExperimental treatment 3 interventions
Group H: Part 6: ABBV-901 + Carboplatin + Bevacizumab ExpansionExperimental treatment 3 interventions

Trial outcomes

Primary outcomes

1

Number of Participants with Adverse Events (AE)

An adverse event (AE) is defined as any untoward medical occurrence in a participant or clinical investigation participant administered a pharmaceutical product, and which does not necessarily have a causal relationship with this treatment.

Time frame
Up to Approximately 3 Years
2

Overall Response (as assessed by the investigator)

Overall response is defined as participants achieving confirmed complete response (CR) or partial response (PR) per Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 as assessed by the investigator.

Time frame
Up to Approximately 3 Years

Secondary outcomes

1

Overall Response (as assessed by independent central review)

Overall response is defined as participants achieving confirmed complete response (CR) or partial response (PR) per Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 as assessed by independent central review (ICR).

Time frame
Up to Approximately 3 Years
2

Duration of Response (DOR)

DOR is defined for participants achieving a confirmed PR or better as the time from the initial response of PR (or better) per investigator review according to RECIST Version 1.1 criteria to disease progression or death of any cause, whichever occurs earlier.

Time frame
Up to Approximately 3 Years
3

Progression-free survival (PFS)

PFS is defined as time from first study treatment to a documented disease progression according to RECIST Version 1.1 (or other assessment criteria), as determined by the investigator, or death due to any cause, whichever occurs earlier.

Time frame
Up to Approximately 3 Years
4

Overall Survival (OS)

OS is defined as time from first study treatment to death due to any cause.

Time frame
Up to Approximately 3 Years

Other outcomes

Sponsors and contacts

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