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NUV-868 as Monotherapy and in Combination With Olaparib or Enzalutamide in Adult Patients With Advanced Solid Tumors

N

Nuvation Bio

Status and phase

Enrolling
Phase 2
Phase 1

Conditions

Prostate Neoplasm
Advanced Solid Tumor
Triple Negative Breast Neoplasms
Cancer of Ovary
Castration Resistant Prostatic Cancer
Castrate Resistant Prostate Cancer
Cancer of Pancreas
Pancreas Neoplasm
Pancreatic Cancer
Cancer of Breast
Breast Cancer
Cancer of the Ovary
Pancreas Cancer
Breast Tumor
Ovarian Cancer
Cancer of the Pancreas
Ovary Cancer
Cancer of the Breast
Castration Resistant Prostatic Neoplasms
Cancer of Prostate
Triple-negative Breast Cancer
Breast Carcinoma
Triple Negative Breast Cancer
Prostatic Cancer
Prostate Cancer
Ovary Neoplasm
Cancer of the Prostate

Treatments

Drug: Enzalutamide
Drug: NUV-868
Drug: Olaparib

Study type

Interventional

Funder types

Industry

Identifiers

NCT05252390
NUV-868-01

Details and patient eligibility

About

NUV-868-01 is a first-in human, open- label, Phase 1/2 dose escalation and expansion study in patients with advanced solid tumors. The Phase 1 and 1b portions include patients with advanced solid tumors and are designed to determine the safety and the dose(s) of NUV-868 to be used as monotherapy and in combination with olaparib or enzalutamide for the Phase 2 portion. In Phase 2, NUV-868 in combination with olaparib or enzalutamide will be given to determine the safety and efficacy of these study treatments. One cohort of patients (with enzalutamide-naïve metastatic castration-resistant prostate cancer) will be randomized to receive either NUV-868 monotherapy, enzalutamide monotherapy, or the combination of NUV-868 + enzalutamide. Patients will self-administer NUV-868 orally daily in 28-day cycles as monotherapy in Phases 1 and 2. In Phases 1b and 2, patients will self-administer NUV-868 orally daily in 28-day cycles in combination with olaparib or enzalutamide daily at standard prescribed doses (Phase 1b) or at the recommended Phase 2 combination dose (RP2cD) that is determined in Phase 1b. Patients will be treated until disease progression, toxicity, withdrawal of consent, or termination of the study.

Enrollment

657 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Key Inclusion Criteria For All Phases and Cohorts:

  1. Recovered from toxicity to prior anticancer therapy
  2. Adequate bone marrow and organ function
  3. No known active or symptomatic central nervous system (CNS) disease

Cohort-Specific Inclusion Criteria: In addition to the inclusion criteria listed above, the following criteria apply for enrollment into specific cohorts.

Phase 1 (NUV-868 Monotherapy)

  1. Patients with advanced solid tumors that have progressed during or after treatment with approved therapies or for which there is no standard effective therapy available
  2. Life expectancy of > 3 months
  3. Eastern Cooperative Oncology Group Performance Status ≤ 2
  4. Measurable or non-measurable disease

Phase 1b (NUV-868 in Combination With Enzalutamide or Olaparib)

  1. Life expectancy of > 3 months

  2. Eastern Cooperative Oncology Group Performance Status ≤ 2

  3. (Select cohorts only) Measurable disease

  4. Patient must be able to read and write sufficiently to document food intake and study drug dosing on the Dosing Diary or must have a caregiver who is willing and able to complete the Dosing Diary with the patient.

  5. One of the following tumor types:

    1. Ovarian: Platinum-resistant OR platinum-refractory high grade serous ovarian, fallopian, or primary peritoneal cancer in the relapsed setting
    2. Pancreatic: Pancreatic ductal adenocarcinoma (PDAC) with progression on or after treatment with at least one line of systemic chemotherapy in the advanced setting
    3. Prostate: Histologically confirmed, metastatic adenocarcinoma of the prostate (adenocarcinoma/high grade carcinoma with neuroendocrine features is allowed) with progression on or after treatment with at least one NHT in the metastatic setting
    4. Breast: Triple-negative breast cancer (TNBC) with progression on or after treatment with at least one line of systemic chemotherapy in the advanced setting
    5. Other advanced tumors (only Phase 1b dose escalation, NUV-868 + olaparib): the study Medical Monitor must approve enrollment.
    6. For all tumor types: Patients will be allowed in the study regardless of their BRCA/HRR status.

Phase 2

  1. Life expectancy of > 6 months

  2. (Select cohorts only): At least one measurable lesion defined by standard criteria

  3. Eastern Cooperative Oncology Group Performance Status ≤ 1

  4. One of the following tumor types:

    1. Ovarian: Platinum-resistant or platinum- refractory high grade serous ovarian, fallopian, or primary peritoneal cancer in the relapsed setting
    2. Pancreatic: Progression on or after treatment with at least one line of systemic chemotherapy in the advanced setting
    3. Prostate: Histologically confirmed, metastatic adenocarcinoma of the prostate (adenocarcinoma/high grade carcinoma with neuroendocrine features is allowed) with progression on or after treatment with at least one NHT in the metastatic setting
    4. Breast: TNBC with progression on or after treatment with at least one line of systemic chemotherapy in the advanced setting

Key Exclusion Criteria For All Phases and Cohorts:

  1. Have received chemotherapy, hormonal therapy (except for ongoing luteinizing hormone-releasing hormone [LHRH] analogs in male patients and premenopausal women), radiation, or biological anticancer therapy within 14 days prior to the first dose of NUV-868.
  2. Received treatment with an investigational agent for any indication within 14 days for non-myelosuppressive agent, or within 21 days or < 5 half-lives (whichever is longer) for myelosuppressive agent, prior to the first dose of study treatment.
  3. Requires medications that are known to be strong (or moderate for olaparib) inducers and/or strong (or moderate for olaparib) inhibitors of CYP3A4/5 enzymes.
  4. Female patients who are pregnant of breastfeeding.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Sequential Assignment

Masking

None (Open label)

657 participants in 7 patient groups

Phase 1 Monotherapy
Experimental group
Description:
NUV-868 will be administered at escalating dose levels until the maximum tolerated dose (MTD) is reached or a recommended Phase 2 dose (RP2D) is determined.
Treatment:
Drug: NUV-868
Phase 1b Combination: NUV-868 + Olaparib
Experimental group
Description:
NUV-868 will be administered at escalating dose levels in combination with olaparib until the recommended Phase 2 combination dose (RP2cD) is determined. 300 mg olaparib will be administered orally twice daily throughout the 28-day cycles of NUV-868.
Treatment:
Drug: Olaparib
Drug: NUV-868
Phase 1b Combination: NUV-868 + Enzalutamide
Experimental group
Description:
NUV-868 will be administered daily at escalating dose levels in combination with enzalutamide until the RP2cD is determined. 160 mg enzalutamide will be administered orally daily throughout the 28-day cycles of NUV-868.
Treatment:
Drug: NUV-868
Drug: Enzalutamide
Phase 2 Combination: NUV-868 + Olaparib
Experimental group
Description:
NUV-868 will be administered at the RP2cD. Olaparib will be administered at the RP2cD.
Treatment:
Drug: Olaparib
Drug: NUV-868
Phase 2 Combination: NUV-868 + Enzalutamide
Experimental group
Description:
NUV-868 will be administered at the RP2cD. Enzalutamide will be administered at the RP2cD.
Treatment:
Drug: NUV-868
Drug: Enzalutamide
Phase 2: NUV-868 Monotherapy
Experimental group
Description:
NUV-868 will be administered at the RP2D in one arm of a randomized Phase 2 combination (NUV-868 + enzalutamide) cohort.
Treatment:
Drug: NUV-868
Phase 2: Enzalutamide Monotherapy
Active Comparator group
Description:
160 mg enzalutamide will be administered orally daily in one arm of a randomized Phase 2 combination (NUV-868 + enzalutamide) cohort.
Treatment:
Drug: Enzalutamide

Trial contacts and locations

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Central trial contact

Nuvation Bio Inc.

Data sourced from clinicaltrials.gov

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