- A Phase 1 Study of ABBV|011 as a Single|Agent and in ...🔍
- A Multicenter🔍
- Genmab and AbbVie Announce Positive Topline Results from ...🔍
- A Phase 1 Study With ABBV|CLS|484 in Subjects With Locally ...🔍
- AbbVie Begins Phase 3 Trial for ABBV|383 in Multiple Myeloma ...🔍
- Phase 1 Asian PK Study of ABBV|CLS|7262🔍
- AbbVie and Bristol|Myers Squibb Announce Clinical Research ...🔍
- A Study Evaluating the Safety🔍
Phase I study of ABBV|428
A Phase 1 Study of ABBV-011 as a Single-Agent and in ...
This is a multicenter, open-label, Phase 1 study of ABBV-011 given as a single agent and in combination with budigalimab (ABBV-181) in participants with ...
A Multicenter, Phase 1/1b, Open-Label, Dose-Escalation Study of ...
Study #2016-0618. A Multicenter, Phase 1/1b, Open-Label, Dose-Escalation Study of ABBV-399, an Antibody Drug Conjugate, in Subjects with Advanced Solid Tumors.
Genmab and AbbVie Announce Positive Topline Results from ...
Company Announcement. Based on the topline results from the EPCORE™ NHL-1 clinical trial, Genmab and AbbVie will engage with global ...
A Phase 1 Study With ABBV-CLS-484 in Subjects With Locally ...
The study will assess the safety, PK, PD, and preliminary efficacy of ABBV-CLS-484 as monotherapy and in combination with a PD-1 targeting agent or with a ...
AbbVie Begins Phase 3 Trial for ABBV-383 in Multiple Myeloma ...
ABBV-383 is being tested in a multicenter, randomized, open-label Phase 3 study, where it is being compared to standard therapies in patients with relapsed or ...
Phase 1 Asian PK Study of ABBV-CLS-7262, an eIF2B Activator ...
Phase 1 Asian PK Study of ABBV-CLS-7262, an eIF2B Activator Being Developed as a Potential Treatment for Amyotrophic Lateral Sclerosis and ...
AbbVie and Bristol-Myers Squibb Announce Clinical Research ...
AbbVie (NYSE: ABBV) and Bristol-Myers Squibb Company (NYSE: BMY) today announced a clinical trial collaboration to evaluate the combination ...
A Study Evaluating the Safety, Pharmacokinetics, and Anti-tumor ...
The study will consist of 2 phases: Dose Escalation Phase and Expansion Phase ... Dose Escalation Phase: Recommended Phase 2 dose (RPTD) for ABBV-321. Time ...
MA09.09 First-In-Human Phase 1 Study of ABBV-399, an Antibody ...
ABBV-399 is a first-in-class ADC composed of ABT-700, an anti–c-Met antibody, conjugated to monomethyl auristatin E (a microtubule inhibitor). Preclinical data ...
REGENXBIO Announces Lancet Publication of Phase I/IIa Study ...
A single ABBV-RGX-314 gene therapy treatment has the potential to become a new standard-of-care option among anti-VEGF treatments by ...
First-in-human phase I study of ABBV-085, an antibody–drug ...
ABBV-085 is a monomethyl auristatin-E antibody–drug conjugate that targets LRRC15 and showed antineoplastic efficacy in preclinical experiments.
A Phase 1 Study With ABBV-CLS-484 in Subjects With Locally ...
Part 1, ABBV-CLS-484 will be administered alone in escalating dose levels to eligible subjects who have advanced solid tumors. Part 2, ABBV-CLS-484 will be ...
AbbVie Launches Phase I Clinical Trial for ABBV-1882, Promising ...
The treatment, ABBV-1882, is a result of meticulous research and development efforts aimed at addressing the complexities of HIV infection. It ...
DEVELOPMENT. ABBV-706 is being investigated in a Phase 1 trial for the treatment of advanced solid tumors, including small cell lung cancer (SCLC), central ...
First-in-human study of ABBV-400, a novel c-Met
The study is also evaluating ABBV-400 with bevacizumab in pts with CRC. Clinical trial information: NCT05029882. Preliminary efficacy outcomes. CRC Dosing ...
A Phase 1 First-in-Human Study Evaluating Safety ... - UroToday
Study Type: Interventional. Clinical Trials Identifier NCT 8-digits: NCT06318273. Sponsor: AbbVie. Phase: Phase 1. Eligibility: Age: minimum 18 ...
Paper: A First-in-Human Phase 1 Study of ABBV-525, a ... - Abstract
3101 A First-in-Human Phase 1 Study of ABBV-525, a Small-Molecule MALT1 Inhibitor, in Patients with Relapsed or Refractory B-Cell Non-Hodgkin ...
Abbvie M20-247: A Phase 1b Study of ABBV-744 Alone or in ...
An investigational drug is one that is not approved by the FDA. Ruxolitinib is approved for the treatment of myelofibrosis. Neither ABBV-744 nor navitoclax is ...
A Phase 1, Multi-center, Open Label First-in-Human Study With ...
The purpose of this study is to see how safe and effective ABBV-CLS-579 is when used alone or in combination with programmed cell death ...
Phase 3: Intravenous (IV) ABBV-383 Monotherapy Versus Standard ...
ABBV-383 is an investigational drug being developed for the treatment of R/R MM. This study is broken into 2 Arms; Arm A and Arm B. .