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Not yet recruitingNCT07778498Updated Aug 21, 2026

A Phase I/II, First-in-Human Study to Evaluate TJ102 in Participants With Advanced or Metastatic Ovarian Cancer and Other Solid Tumors.

A Phase 1/2 interventional study of TJ102 in Ovarian Cancer, sponsored by Phrontline Biopharma. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-21.

Sponsored by Phrontline Biopharma · Phase 1/2, Interventional, and Treatment

Phase
Phase 1/2
Study type
Interventional
Enrollment
150
Allocation
Not applicable
Ages
18 Years and older
Sex
All
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Study summary

The goal of this clinical trial is to evaluate whether TJ102, an investigational antibody-drug conjugate (ADC), can safely and effectively treat patients with advanced ovarian or other solid tumors. The main objectives of this study are : • To Determine the maximum tolerated dose (MTD) and recommended dose for expansion (RDE) of TJ102 • to show preliminary antitumor activity in patients with advanced ovarian or other solid tumors. Participants will: • Receive intravenous (IV) infusions of TJ102 at escalating dose levels (during dose escalation) or at the selected expansion dose. • Undergo regular tumor imaging to assess response. • Provide blood samples for pharmacokinetics (PK) and biomarker analysis. • Be monitored for side effects and overall tolerability. This study is being conducted in adult patients with advanced or metastatic ovarian or other solid tumors who have exhausted standard treatment options.

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Conditions studied

  • Ovarian Cancer

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Main Inclusion Criteria:

  1. Has histologically or cytologically documented locally advanced or metastatic high-grade serous epithelial ovarian cancer, including ovarian, fallopian tube, or primary peritoneal carcinoma, that is not amenable to curative surgery or radiotherapy, and has demonstrated radiographic disease progression on the most recent line of systemic therapy.
  2. Prior exposure to a platinum-containing regimen is mandatory. Platinum-resistant disease is defined as disease progression during or within 6 months following completion of the most recent platinum-containing regimen. Patients with platinum-sensitive disease may be eligible during Phase 1 if they have received at least 2 prior lines of platinum-containing systemic therapy.
  3. Prior Lines of therapy:

    Subjects must have received at least one (≥1) and no more than four (≤4) prior lines of systemic therapy in the advanced or metastatic setting and have progressed on, been intolerant to, or be ineligible for standard therapies available in their local region. Prior treatment with mirvetuximab soravtansine and/or bevacizumab is permitted but not required, reflecting regional differences in standard of care, regulatory approval status, availability, or access.

    Hormonal therapy and maintenance therapy, including PARP inhibitors or bevacizumab maintenance, are not counted as prior lines of systemic therapy unless administered for treatment of progressive disease.

  4. Have at least one measurable lesion by RECIST v1.1 (Eisenhauer et al., 2009) for solid tumors;
  5. ≥18 years old;
  6. Eastern Cooperative Oncology Group (ECOG) performance status (Oken et al., 1982) of 0 to 1;
  7. Life expectancy of ≥12 weeks;
  8. Patients with adequate organ function and the laboratory test criteria specifically defined as follows within 7 days prior to the first dosing;

Main Exclusion Criteria:

  1. Has know hypersensitivity to any component of TJ102 or has a history of severe hypersensitivity reactions to other monoclonal antibodies.
  2. Has received more than two (2) prior antibody-drug conjugate (ADC) therapies in the advanced or metastatic disease setting, including ADCs containing topoisomerase I inhibitor payloads (e.g., SN-38, DXd, exatecan derivatives) or antimicrotubule payloads (e.g., MMAE, DM1/DM4, auristatins, maytansinoids).
  3. Prior therapy with any antibody-drug conjugate (ADC) whose cytotoxic payload is eribulin or a structural derivative thereof is prohibited in the advanced/metastatic disease setting.
  4. Has received mitomycin and nitrosoureas treatment within 6 weeks prior to the first administration; oral fluorouracil-like drugs such as S-1, capecitabine, or palliative radiotherapy within 2 weeks prior to the first administration; Has received other chemotherapy, biological therapy, major surgery, radical radiotherapy, targeted therapy (including small molecule inhibitor of tyrosine kinase) and other anti-tumor therapy within 5 half-lives or 28 days, whichever is shorter, prior to the first administration of TJ102; Has received anti-tumor herbal medicine within 14 days prior to first dose of TJ102;
  5. Has received a strong or moderate CYP3A4 inhibitor within 3 half-lives prior to first dose of TJ102;
  6. Received an investigational drug within 28 days or 2 half-lives (whichever is shorter) prior to first dose of TJ102; Current participation in other interventional clinical studies (participation in survival follow-up is allowed);
  7. Toxic effects of prior anti-tumor therapy have not recovered to NCI-CTCAE V6.0 Grade ≤1 (excluding alopecia and skin pigmentation). Subject with irreversible toxicities caused by prior anti-tumor therapy (eg, hearing loss) that will not increase the safety risk may be eligible per the discretion of the Investigator;
  8. Has a history of (non-infectious) interstitial lung disease (ILD) that required steroids, has current ILD/pneumonitis, or where suspected ILD/pneumonitis can't be ruled out by imaging at screening;
  9. Presence of severe dry eye syndrome, severe keratitis, severe conjunctivitis, or other severe conditions that may increase the risk of corneal epithelial damage at the discretion of investigator;
  10. Presence of Grade ≥2 or history of Grade ≥3 peripheral neuropathy.
  11. Uncontrolled or significant cardiovascular disease
  12. For patients with documented positive virology status, as confirmed by Screening hepatitis B virus (HBV), hepatitis C virus (HCV) and human immunodeficiency virus (HIV) tests, only the following patients may be eligible as evaluated by the sponsor and investigator:

    Patients with active hepatitis B: HBV DNA ≤500 IU/mL during Screening. Patients who are hepatitis C virus antibody positive (HCV Ab+), should have controlled infection (HCV RNA≤ULN by polymerase chain reaction [PCR] either spontaneously or in response to a successful prior course of anti-HCV therapy at Screening). Patients with controlled infections must undergo periodic monitoring of HCV RNA as per treating physician.

  13. Severe infection, including but not limited to hospitalization due to infection, bacteraemia, or severe pneumonia complications, occurs within 4 weeks prior to initiation of study treatment; Or patients who received therapeutic oral or intravenous antibiotics and who received prophylactic antibiotics (e.g., for the prevention of urinary tract infection or chronic obstructive pulmonary disease) within two weeks prior to starting study treatment.
  14. Active central nervous system (CNS) metastases or meningeal metastases. Subjects may be enrolled in the study if their CNS metastases have received adequate local therapy and have been clinical stable for at least 4 weeks (i.e., imaging shows no progression of the brain lesion and neurologically relevant symptoms are stable), and require a dose of prednisone of ≤20 mg/day (or equivalent dose). Subjects with untreated CNS metastases are excluded.
  15. Other malignancies within 3 years prior to initiation of study treatment (Note: does not include tumors with a negligible risk for metastasis or death, eg, non-melanoma basal cell carcinoma or squamous cell carcinoma of the skin, breast/cervical carcinoma in situ, superficial bladder carcinoma that have received radical treatment and without evidence of disease recurrence);
  16. Female patients who are lactating or breastfeeding;
  17. The investigator believes that the subject may have other factors that may affect the results of the study and interfere with the subject's participation in the entire study process, including previous or existing physical conditions, abnormal treatment or laboratory tests, and the subject's unwillingness to comply with all procedures, restrictions, and requirements of the study.
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Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
150 participants (estimated)

Study arms

  • Experimental
    TJ102

    TJ102 will be infused intravenously once every 3 weeks. Participants will receive TJ102 at escalating dose levels (during dose escalation) or at the selected expansion dose

    Biological: TJ102

Interventions

  • BiologicalTJ102

    TJ102 is a CDH6/FRa directed antibody conjugate with dual payloads

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What researchers measure

Primary outcomes

  1. Number of participants with Dose-limiting toxicities

    Time frame: 2 years

  2. Number of participants with treatment-emergent adverse events (TEAEs)

    Time frame: 2 years

  3. Number of participants with treatment-related adverse events (TRAEs)

    Time frame: 2 years

Secondary outcomes

  1. Objective response rate (ORR)

    Time frame: 2 years

  2. Progression-free survival (PFS)

    Time frame: 2 years

  3. Overall survival (OS)

    Time frame: 2 years

  4. Duration of response (DoR)

    Time frame: 2 years

  5. Maximum observed concentration (Cmax)

    Measuring maximum drug concentration in blood after study treatment

    Time frame: 1 year

  6. Time to Cmax (Tmax)

    Measuring time to reach maximum drug concentration in blood after study treatment

    Time frame: 1 year

  7. Area under the concentration versus time curve (AUC)

    Measuring area under the drug concentration versus time curve

    Time frame: 1 year

  8. half-life time (t1/2)

    Measuring the time for the drug concentration to reach half of its value

    Time frame: 1 year

  9. Clearance (CL)

    Measuring the apparent volume of plasma completely cleared of drug per unit of time

    Time frame: 1 year

  10. Volume of distribution

    Measuring the distribution of drugs in the body as relative to the measured concentration.

    Time frame: 1 year

  11. Elimination rate constant (λz)

    Measuring the fraction of drug eliminated per unit of time

    Time frame: 1 year

  12. Mean residence time (MRT)

    Measuring the average duration that the study drug remains in the body

    Time frame: 1 year

  13. Proportion of participants with anti-drug antibodies (ADA) and neutralizing antibodies (NAb) if applicable

    Time frame: 2 years

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Registry details

Key details

Study ID
NCT07778498
Lead sponsor
Phrontline Biopharma
Responsible party
Sponsor
First posted
Aug 21, 2026
Start date
Sep 15, 2026 (estimated)
Primary completion
Sep 2029 (estimated)
Completion
Sep 2030 (estimated)
Last update
Aug 21, 2026

Study contacts

Medical Director
Contact
lisong.yang@phrontlinebio.com
086-13166137296

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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