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A Study to Evaluate the Efficacy and Safety of TL118 in Solid Tumors Patients

  • PhasePhase 2
  • StatusRecruiting
  • Planned enrollment60 people
  • Recruiting US sites4
  • SponsorTeligene US
  • RegistryNCT06010342

Recruitment re-checked on ClinicalTrials.gov Oct 30, 2026. Public record; not medical advice.

A Study to Evaluate the Efficacy and Safety of TL118 in Solid Tumors Patients: a one-minute explainerNCT060103421 min

Eligibility

Who can join

The film gives the main points. The full list below is copied from the registry; the study team makes the final decision.

  • Age18 Years to no maximum
  • SexAll
  • Healthy volunteersNo

You may be able to join if

  • Age 18 years old and above, male or female
  • Histologically or cytologically confirmed diagnosis of locally advanced or metastatic solid tumor that harbors an NTRK1/2/3 gene fusion that is predicted to translate into a fusion protein with a functional tropomyosin receptor kinase (TRK)A/B/C kinase domain, without a concomitant second onco-driver
  • Patients must have had disease progression during or after prior treatment for their tumor, or would be unlikely to tolerate or derive clinical benefit from appropriate standard of care therapy or are not suitable - in the opinion of the Investigator - to receive standard of care therapy; prior treatment with approved or investigational TRK inhibitors is not allowed, except for prior TRK treatment for less than 28 days due to intolerable toxicity)
  • At least one measurable lesion
  • Eastern Cooperative Oncology Group (ECOG) score of 0, 1, or 2
  • A minimum life expectancy of > 3 months
  • Adequate bone marrow reserve, hepatic, renal, and coagulation function
  • Other inclusion criteria apply for participating in the Study

You cannot join if

  • Any systemic anti-tumor therapy such as chemotherapy and radiation therapy (including curative radiotherapy or spinal radiotherapy portion > 30%) used within 3 weeks prior to enrollment; immunotherapy within 4 weeks; any palliative radiotherapy for non-target lesions used to relieve symptoms and traditional Chinese medicines (TCMs) indicated for the tumor (including Chinese patent medicine) within 2 weeks prior to enrollment
  • Participation in another interventional clinical trial 2 weeks prior to enrollment or within 5 half-lives from the last dose of IP (whichever is shorter)
  • Any unresolved toxicities from prior therapy greater than Grade 1, at the time of screening with the exception of toxicities posing no safety risk in the opinion of the Investigator
  • Active central nervous system metastases
  • Any other primary malignant tumors within 3 years (except for cured skin basal cell carcinoma and carcinoma in situ of cervix, low-risk cancer
  • Any active infection which has not been controlled at screening
  • Other exclusion criteria apply for participating in the Study

The treatment

How it is intended to work

This is how the treatment is meant to work. Whether it helps, and how safe it is, is what this trial is testing.

Treatments listed in the registry

  • TL118 Capsule (Drug): Oral administration

The study

Treatment groups

Na · Single Group · masking: None

Single arm, Open label (Experimental)

Participants will receive TL118 capsule taken orally with (preferred) or without food, 252 mg twice daily, 28 days for a cycle.

Goals

What the study measures

Main goals

  • Objective Response Rate (ORR) (Pre-dose up to approximately 24 months post-dose)

Other goals

  • Duration of Response (DoR)
  • Disease Control Rate (DCR)
  • Progression Free Survival (PFS)
  • Time to Tumor Progression (TTP)
  • Time to Response (TTR)
  • Time to Treatment Failure (TTF)
  • Overall Survival (OS)
  • 1-year Progression Free Survival
  • 1-year Survival
  • Number of Participants Experiencing Adverse Events (AE)
  • Number of Participants Experiencing Adverse Drug Reactions (ADR)
  • Number of Participants Experiencing Serious Adverse Events (SAE)
  • Number of Participants Experiencing Serious Adverse Reactions (SAR)
  • Area Under The Curve (AUC) of TL118
  • Maximum Plasma Concentration (Cmax) of TL118
  • Minimum Plasma Concentration (Cmin) of TL118
  • Time to Peak Drug Concentration (Tmax) of TL118
  • TL118 half-life (T1/2)
  • Apparent Clearance (CL/f) of TL118
  • Volume of Distribution (Vz/F) of TL118

Planned enrollment: 60 (estimated).

Where

Recruiting US sites

  • Adventist Health Glendale, Glendale, California
  • Texas Oncology Dallas, Dallas, Texas
  • The University of Texas MD Anderson Cancer Center, Houston, Texas
  • Texas Oncology Lewisville Castle Hills, Lewisville, Texas

16 recruiting sites outside the US. Site status as of Oct 30, 2026. Check the live record before contacting a site.

Sources

Where this comes from

Registry record reviewed as fetched Oct 30, 2026, last updated by the sponsor Oct 26, 2026. Public record; not medical advice.

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