ClinicalTrials.gov record
Completed Phase 1 Interventional

Continuation Study of Lapatinib Monotherapy or Lapatinib in Combination With Other Anti-cancer Agents

ClinicalTrials.gov ID: NCT00790816

Public ClinicalTrials.gov record NCT00790816. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Apr 29, 2026, 12:48 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-Label Phase Ib Continuation Study of Lapatinib Monotherapy or Lapatinib in Combination With Other Anti-Cancer Treatment in Patients With Solid Tumors

Study identification

NCT ID
NCT00790816
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
500 participants

Conditions and interventions

Interventions

  • Lapatinib Drug
  • Lapatinib in combination with an anti-cancer agent Drug
  • Lapatinib in combination with an anti-cancer agent as specified by parent protocol Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 30, 2008
Primary completion
Aug 18, 2016
Completion
Aug 18, 2016
Last update posted
Feb 27, 2018

2008 – 2016

United States locations

U.S. sites
15
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
Novartis Investigative Site Scottsdale Arizona 85259
Novartis Investigative Site Tucson Arizona 85724
Novartis Investigative Site Santa Monica California 90404
Novartis Investigative Site Washington D.C. District of Columbia 20007
Novartis Investigative Site Fort Myers Florida 33916
Novartis Investigative Site Atlanta Georgia 30341
Novartis Investigative Site Detroit Michigan 48202
Novartis Investigative Site Lebanon New Hampshire 03756
Novartis Investigative Site Buffalo New York 14263
Novartis Investigative Site Durham North Carolina 27710
Novartis Investigative Site Cleveland Ohio 44106
Novartis Investigative Site Greenville South Carolina 29605
Novartis Investigative Site Memphis Tennessee 38120
Novartis Investigative Site Nashville Tennessee 37203
Novartis Investigative Site Salt Lake City Utah 84112

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 8 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00790816, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 27, 2018 · Synced Apr 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00790816 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →