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NCT ID	NCT05029882
Title	Study to Assess Adverse Events and Change in Disease Activity in Adult Participants With Advanced Solid Tumors Receiving Intravenous (IV) ABBV-400 as Monotherapy and in Combination With IV Bevacizumab
Recruitment	Recruiting
Gender	both
Phase	Phase I
Variant Requirements	Yes
Sponsors	AbbVie
Indications	colorectal cancer lung non-small cell carcinoma renal cell carcinoma gastroesophageal junction adenocarcinoma head and neck squamous cell carcinoma Advanced Solid Tumor
Therapies	ABBV-400 + Bevacizumab ABBV-400 Bevacizumab + Trifluridine-tipiracil hydrochloride
Age Groups:	adult \| senior
Covered Countries	USA \| POL \| ISR \| FRA \| ESP \| AUS