A Study of DR-0202 in Patients With Locally Advanced or Metastatic, Relapsed or Refractory Carcinomas

Part of paid clinical trials in Denver, Colorado.

Sponsor
Dren Bio
Study ID
NCT06999187
Phase
PHASE1
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • DR-0202 — DRUG
    DR-0202 is a bispecific antibody

Study Details

A phase 1a/1b, multicenter, open-label, dose escalation/expansion, multiple-dose study to evaluate the safety and activity of DR-0202 in patients with locally advanced or metastatic, relapsed or refractory carcinomas

Key Dates

Start date
Jun 3, 2025
Status verified
Aug 2025
Primary completion
Jul 31, 2027
Completion
Dec 31, 2027

Study Design

Enrollment
96 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT

Arms

  • Experimental: DL1 of DR-0202
    Participants in this arm will receive DL1 milligrams of DR-0202 every 2 weeks until progression or withdrawal
  • Experimental: DL2 of DR-0202
    Participants in this arm will receive DL2 milligrams of DR-0202 every 2 weeks until progression or withdrawal
  • Experimental: DL3 of DR-0202
    Participants in this arm will receive DL3 milligrams of DR-0202 every 2 weeks until progression or withdrawal
  • Experimental: DL4 of DR-0202
    Participants in this arm will receive DL4 milligrams of DR-0202 every 2 weeks until progression or withdrawal
  • Experimental: DL5 of DR-0202
    Participants in this arm will receive DL5 milligrams of DR-0202 every 2 weeks until progression or withdrawal
  • Experimental: DL6 of DR-0202
    Participants in this arm will receive DL6 milligrams of DR-0202 every 2 weeks until progression or withdrawal
  • Experimental: DL7 of DR-0202
    Participants in this arm will receive DL7 milligrams of DR-0202 every 2 weeks until progression or withdrawal
  • Experimental: DL8 of DR-0202
    Participants in this arm will receive DL8 milligrams of DR-0202 every 2 weeks until progression or withdrawal

Primary Outcome Measure

Incidence, severity, and relationship of treatment-emergent adverse events (TEAEs) as assessed by CTCAE v5.0 during DR-0202 treatment through study completion (Safety and Tolerability) [ Time Frame: 28-day DLT Period and Treatment Duration / Study Completion ]

Central Contacts

Locations (10)

FacilityCityStateZIPSite coordinators
Dren Investigational SiteDenverColorado80218
Dren Bio Central Contact
415-737-5277
Dren Investigational SiteOrlandoFlorida32827
Dren Bio Central Contact
415-737-5277
Dren Investigational SiteSarasotaFlorida34232
Dren Bio Central Contact
415-737-5277
Dren Investigational SiteHuntersvilleNorth Carolina28078
Dren Bio Central Contact
415-737-5277
Dren Investigational SiteOklahoma CityOklahoma73104
Dren Bio Central Contact
415-737-5277
Dren Investigational SiteGreenvilleSouth Carolina29605
Dren Bio Central Contact
415-737-5277
Dren Investigational SiteAustinTexas78758
Dren Bio Central Contact
415-737-5277
Dren Investigational SiteDallasTexas75230
Dren Bio Central Contact
415-737-5277
Dren Investigational SiteSan AntonioTexas78229
Dren Bio Central Contact
415-737-5277
Dren Investigational SiteFairfaxVirginia22031
Dren Bio Central Contact
415-737-5277

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