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Company

AbbVie

Pharmaceutical intelligence for AbbVie with 53 indexed intelligence signals across regulatory, clinical, competitive, and market developments.

Signals
32
Catalysts
21
Assets
31

Recent signals(32)

RegulatoryAugust 4, 2026

FDA Accepts Supplement for Lupron by AbbVie

The FDA has accepted a supplemental application for Lupron (leuprolide acetate) from AbbVie.

ClinicalAugust 3, 2026

Study on Guselkumab Therapy's Impact on NAFLD in PsA Patients

The study investigates the effects of Guselkumab on disease severity in PsA patients with NAFLD.

RegulatoryJuly 31, 2026

FDA Accepts Supplement Application for HADLIMA by Samsung Bioepis

The FDA has accepted the supplemental application for HADLIMA (BLA761059), a biosimilar to adalimumab.

Upcoming catalysts(1)

Phase II Readout

AbbVie — Emraclidine

Second-wave muscarinic data will clarify class viability post-KarXT launch.

September 18, 2026 · Phase II

Regulatory activity(15)

RegulatoryAugust 4, 2026

FDA Accepts Supplement for Lupron by AbbVie

The FDA has accepted a supplemental application for Lupron (leuprolide acetate) from AbbVie.

RegulatoryJuly 31, 2026

FDA Accepts Supplement Application for HADLIMA by Samsung Bioepis

The FDA has accepted the supplemental application for HADLIMA (BLA761059), a biosimilar to adalimumab.

RegulatoryJuly 29, 2026

FDA Approves Supplemental Application for KALETRA by AbbVie

The FDA has approved a supplemental application for KALETRA, a combination of Lopinavir and Ritonavir, submitted by AbbVie.

Clinical activity(13)

ClinicalAugust 3, 2026

Study on Guselkumab Therapy's Impact on NAFLD in PsA Patients

The study investigates the effects of Guselkumab on disease severity in PsA patients with NAFLD.

ClinicalJuly 19, 2026

Epcoritamab Trial in Japanese R/R B-Cell NHL Shows Safety and Efficacy Potential

A trial is underway to assess the safety and efficacy of epcoritamab in Japanese patients with relapsed or refractory B-cell non-Hodgkin lymphoma.

ClinicalJuly 7, 2026

Janssen's Guselkumab Compared to Risankizumab in Crohn's Disease Study Initiated

A clinical trial has been initiated to compare the efficacy of guselkumab and risankizumab in treating moderately to severely active Crohn's Disease.

Competitive activity(4)

CompetitiveJuly 26, 2026

B2227 vs. Vraylar: Pharmacokinetics Study in Schizophrenia Launched

A new study has been initiated to compare the pharmacokinetics of B2227 Extended-Release Injectable Suspension with Vraylar® in schizophrenia patients.

CompetitiveJuly 23, 2026

AbbVie Initiates Study on Surzetoclax for Relapsed/Refractory Multiple Myeloma

AbbVie is conducting a study to evaluate the safety and efficacy of surzetoclax in combination with other agents for relapsed/refractory multiple myeloma.

CompetitiveJune 28, 2026

AbbVie Evaluates AGN-151586 with BOTOX for Glabellar Lines in New Trial

A new clinical trial is assessing the safety and efficacy of AGN-151586 in combination with BOTOX for treating glabellar lines.

Assets

ABBV-722 →
ABBV-932 →
AGN-151586 →
Atogepant →
Botox →
daratumumab →
DECNUPAZ →
Dermatology →
dupilumab →
Dupixent →
Emraclidine →
Genmab →
Guselkumab →
HADLIMA →
Humira →
Ibrutinib →

Therapeutic areas

Aesthetic Medicine →
Antiviral →
Atopic Dermatitis →
Autoimmune Disease →
B-Cell Non-Hodgkin Lymphoma →
BCL-2 Inhibitor →
Biosimilar →
Bipolar Disorder →
CLL →
Crohn's Disease →
Dermatology →
Dermatology · Aesthetic Medicine →
Dermatology · Atopic Dermatitis →

Indications

Autoimmune Disease →
B-Cell Non-Hodgkin Lymphoma →
Bipolar Disorder →
Crohn's Disease →
Infectious Disease →
Psoriatic Arthritis →
Schizophrenia →

Newsletter

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Regulatory
July 29, 2026

FDA Approves Supplemental Application for KALETRA by AbbVie

The FDA has approved a supplemental application for KALETRA, a combination of Lopinavir and Ritonavir, submitted by AbbVie.

RegulatoryJuly 29, 2026

FDA Accepts Supplemental Application for Norvir (Ritonavir) by AbbVie

The FDA has accepted a supplemental application for Norvir (Ritonavir) submitted by AbbVie.

CompetitiveJuly 26, 2026

B2227 vs. Vraylar: Pharmacokinetics Study in Schizophrenia Launched

A new study has been initiated to compare the pharmacokinetics of B2227 Extended-Release Injectable Suspension with Vraylar® in schizophrenia patients.

RegulatoryJuly 25, 2026

FDA Accepts Supplement for RINVOQ (Upadacitinib) by AbbVie

The FDA has accepted a supplemental application for RINVOQ (upadacitinib), indicating ongoing development and potential label expansion.

CompetitiveJuly 23, 2026

AbbVie Initiates Study on Surzetoclax for Relapsed/Refractory Multiple Myeloma

AbbVie is conducting a study to evaluate the safety and efficacy of surzetoclax in combination with other agents for relapsed/refractory multiple myeloma.

RegulatoryJuly 20, 2026

FDA Grants Priority Review for ABBVIE's BLA761460 (DECNUPAZ)

The FDA has granted priority review for ABBVIE's Biologics License Application for DECNUPAZ (BLA761460).

RegulatoryJuly 20, 2026

FDA Accepts Supplemental NDA for Linzess by AbbVie

The FDA has accepted a supplemental NDA for Linzess (linaclotide) submitted by AbbVie, indicating a priority review.

ClinicalJuly 19, 2026

Epcoritamab Trial in Japanese R/R B-Cell NHL Shows Safety and Efficacy Potential

A trial is underway to assess the safety and efficacy of epcoritamab in Japanese patients with relapsed or refractory B-cell non-Hodgkin lymphoma.

RegulatoryJuly 19, 2026

FDA Accepts Supplemental NDA for VENCLEXTA by AbbVie

The FDA has accepted a supplemental NDA for VENCLEXTA (venetoclax) from AbbVie.

RegulatoryJuly 13, 2026

FDA Accepts Supplemental Application for Lupron by AbbVie

The FDA has accepted a supplemental application for Lupron, an injectable hormonal therapy.

RegulatoryJuly 11, 2026

FDA Accepts Supplement Application for HADLIMA (Adalimumab Biosimilar)

The FDA has accepted the supplemental application for HADLIMA, a biosimilar to adalimumab.

RegulatoryJuly 10, 2026

FDA Approves Supplemental Application for RINVOQ LQ by AbbVie

The FDA has approved a supplemental application for RINVOQ LQ (upadacitinib) submitted by AbbVie.

ClinicalJuly 7, 2026

Janssen's Guselkumab Compared to Risankizumab in Crohn's Disease Study Initiated

A clinical trial has been initiated to compare the efficacy of guselkumab and risankizumab in treating moderately to severely active Crohn's Disease.

ClinicalJuly 7, 2026

APT Comparison Study to Evaluate Atogepant vs. Topiramate and Propranolol for Migraine Prevention

The APT Comparison Study will evaluate the effectiveness and tolerability of atogepant against topiramate and propranolol in migraine prevention.

RegulatoryJuly 3, 2026

FDA Accepts Supplement for SKYRIZI (Risankizumab) by AbbVie

The FDA has accepted a supplemental application for SKYRIZI (Risankizumab) from AbbVie.

ClinicalJuly 1, 2026

AbbVie Initiates Study on Surabgene Lomparvovec for Neovascular AMD

AbbVie is conducting a study to evaluate the safety and efficacy of Surabgene Lomparvovec in adults with neovascular age-related macular degeneration.

CompetitiveJune 28, 2026

AbbVie Evaluates AGN-151586 with BOTOX for Glabellar Lines in New Trial

A new clinical trial is assessing the safety and efficacy of AGN-151586 in combination with BOTOX for treating glabellar lines.

ClinicalJune 27, 2026

AbbVie Initiates Phase 2b/3 Trial of Surabgene Lomparvovec for Diabetic Retinopathy

AbbVie is conducting Phase 2b/3 clinical trial to evaluate surabgene lomparvovec as a gene therapy for diabetic retinopathy.

CompetitiveJune 26, 2026

AbbVie Trials Upadacitinib for Moderate-to-Severe Atopic Dermatitis in Dupilumab Inadequate Responders

A new clinical trial is evaluating upadacitinib in adults with moderate-to-severe atopic dermatitis who have not responded adequately to dupilumab.

ClinicalJune 26, 2026

Phase 1 Study of ABBV-722 Shows Focus on Safety and Pharmacokinetics

AbbVie is conducting Phase 1 study to assess the safety, tolerability, and pharmacokinetics of ABBV-722 in healthy adults.

ClinicalJune 25, 2026

AbbVie initiates pediatric study of Risankizumab for Ulcerative Colitis

A new study is underway to evaluate the safety and efficacy of Risankizumab in pediatric patients with moderate to severe Ulcerative Colitis.

ClinicalJune 24, 2026

AbbVie initiates trial for ubrogepant in menstrual migraine treatment

AbbVie is conducting a study to evaluate the safety and efficacy of ubrogepant for treating menstrual migraine in adult women.

ClinicalJune 20, 2026

AbbVie initiates trial for telisotuzumab adizutecan in mCRC with FOLFOX and bevacizumab/panitumumab

A new study is evaluating the efficacy and safety of telisotuzumab adizutecan in combination with standard mCRC treatments.

ClinicalJune 19, 2026

AbbVie Initiates Trial for ABBV-932 in Bipolar Disorder Depressive Episodes

AbbVie is conducting a trial to evaluate the safety and efficacy of ABBV-932 in adults with depressive episodes linked to bipolar I or II disorder.

ClinicalJune 19, 2026

AbbVie Evaluates XEN63 Gel Stent for Glaucoma via Two Surgical Approaches

A clinical trial is underway to assess the safety and effectiveness of the XEN63 gel stent in glaucoma patients using two different surgical approaches.

RegulatoryJune 18, 2026

FDA Accepts Supplement Application for SKYRIZI (Risankizumab)

The FDA has accepted a supplemental application for SKYRIZI, indicating ongoing development and potential label expansion.

RegulatoryJune 18, 2026

FDA Accepts Supplement Application for SKYRIZI (Risankizumab) by AbbVie

The FDA has accepted a supplemental application for SKYRIZI (Risankizumab) from AbbVie.

RegulatoryJune 17, 2026

FDA Lists Quinacrine Hydrochloride for Compounding in Cutaneous Lupus Erythematosus

Quinacrine is included on the FDA 503B list for compounding, indicating a clinical need for its use in treating cutaneous lupus erythematosus.

ClinicalJune 17, 2026

Study Evaluates Outcomes After Discontinuation of BTK Inhibitors in CLL Patients

A Phase II study is assessing the outcomes of stopping BTK inhibitor therapy in CLL patients in remission for over two years.

Regulatory
July 29, 2026

FDA Accepts Supplemental Application for Norvir (Ritonavir) by AbbVie

The FDA has accepted a supplemental application for Norvir (Ritonavir) submitted by AbbVie.

RegulatoryJuly 25, 2026

FDA Accepts Supplement for RINVOQ (Upadacitinib) by AbbVie

The FDA has accepted a supplemental application for RINVOQ (upadacitinib), indicating ongoing development and potential label expansion.

RegulatoryJuly 20, 2026

FDA Grants Priority Review for ABBVIE's BLA761460 (DECNUPAZ)

The FDA has granted priority review for ABBVIE's Biologics License Application for DECNUPAZ (BLA761460).

RegulatoryJuly 20, 2026

FDA Accepts Supplemental NDA for Linzess by AbbVie

The FDA has accepted a supplemental NDA for Linzess (linaclotide) submitted by AbbVie, indicating a priority review.

RegulatoryJuly 19, 2026

FDA Accepts Supplemental NDA for VENCLEXTA by AbbVie

The FDA has accepted a supplemental NDA for VENCLEXTA (venetoclax) from AbbVie.

RegulatoryJuly 13, 2026

FDA Accepts Supplemental Application for Lupron by AbbVie

The FDA has accepted a supplemental application for Lupron, an injectable hormonal therapy.

RegulatoryJuly 11, 2026

FDA Accepts Supplement Application for HADLIMA (Adalimumab Biosimilar)

The FDA has accepted the supplemental application for HADLIMA, a biosimilar to adalimumab.

RegulatoryJuly 10, 2026

FDA Approves Supplemental Application for RINVOQ LQ by AbbVie

The FDA has approved a supplemental application for RINVOQ LQ (upadacitinib) submitted by AbbVie.

RegulatoryJuly 3, 2026

FDA Accepts Supplement for SKYRIZI (Risankizumab) by AbbVie

The FDA has accepted a supplemental application for SKYRIZI (Risankizumab) from AbbVie.

RegulatoryJune 18, 2026

FDA Accepts Supplement Application for SKYRIZI (Risankizumab)

The FDA has accepted a supplemental application for SKYRIZI, indicating ongoing development and potential label expansion.

RegulatoryJune 18, 2026

FDA Accepts Supplement Application for SKYRIZI (Risankizumab) by AbbVie

The FDA has accepted a supplemental application for SKYRIZI (Risankizumab) from AbbVie.

RegulatoryJune 17, 2026

FDA Lists Quinacrine Hydrochloride for Compounding in Cutaneous Lupus Erythematosus

Quinacrine is included on the FDA 503B list for compounding, indicating a clinical need for its use in treating cutaneous lupus erythematosus.

ClinicalJuly 7, 2026

APT Comparison Study to Evaluate Atogepant vs. Topiramate and Propranolol for Migraine Prevention

The APT Comparison Study will evaluate the effectiveness and tolerability of atogepant against topiramate and propranolol in migraine prevention.

ClinicalJuly 1, 2026

AbbVie Initiates Study on Surabgene Lomparvovec for Neovascular AMD

AbbVie is conducting a study to evaluate the safety and efficacy of Surabgene Lomparvovec in adults with neovascular age-related macular degeneration.

ClinicalJune 27, 2026

AbbVie Initiates Phase 2b/3 Trial of Surabgene Lomparvovec for Diabetic Retinopathy

AbbVie is conducting Phase 2b/3 clinical trial to evaluate surabgene lomparvovec as a gene therapy for diabetic retinopathy.

ClinicalJune 26, 2026

Phase 1 Study of ABBV-722 Shows Focus on Safety and Pharmacokinetics

AbbVie is conducting Phase 1 study to assess the safety, tolerability, and pharmacokinetics of ABBV-722 in healthy adults.

ClinicalJune 25, 2026

AbbVie initiates pediatric study of Risankizumab for Ulcerative Colitis

A new study is underway to evaluate the safety and efficacy of Risankizumab in pediatric patients with moderate to severe Ulcerative Colitis.

ClinicalJune 24, 2026

AbbVie initiates trial for ubrogepant in menstrual migraine treatment

AbbVie is conducting a study to evaluate the safety and efficacy of ubrogepant for treating menstrual migraine in adult women.

ClinicalJune 20, 2026

AbbVie initiates trial for telisotuzumab adizutecan in mCRC with FOLFOX and bevacizumab/panitumumab

A new study is evaluating the efficacy and safety of telisotuzumab adizutecan in combination with standard mCRC treatments.

ClinicalJune 19, 2026

AbbVie Initiates Trial for ABBV-932 in Bipolar Disorder Depressive Episodes

AbbVie is conducting a trial to evaluate the safety and efficacy of ABBV-932 in adults with depressive episodes linked to bipolar I or II disorder.

ClinicalJune 19, 2026

AbbVie Evaluates XEN63 Gel Stent for Glaucoma via Two Surgical Approaches

A clinical trial is underway to assess the safety and effectiveness of the XEN63 gel stent in glaucoma patients using two different surgical approaches.

ClinicalJune 17, 2026

Study Evaluates Outcomes After Discontinuation of BTK Inhibitors in CLL Patients

A Phase II study is assessing the outcomes of stopping BTK inhibitor therapy in CLL patients in remission for over two years.

CompetitiveJune 26, 2026

AbbVie Trials Upadacitinib for Moderate-to-Severe Atopic Dermatitis in Dupilumab Inadequate Responders

A new clinical trial is evaluating upadacitinib in adults with moderate-to-severe atopic dermatitis who have not responded adequately to dupilumab.

Janssen →
KALETRA →
Linzess →
Lupron →
Norvir (Ritonavir) →
Quinacrine Hydrochloride →
Ranibizumab →
RINVOQ →
Risankizumab →
SKYRIZI →
Surabgene Lomparvovec →
Trial Update →
VENCLEXTA →
XEN63 →
Xeomin →
Dermatology · Autoimmune Disease →
Endocrinology →
Endocrinology · Hormonal Therapy →
Gastroenterology →
Gastroenterology · Chronic Anal Fissure →
Gastroenterology · Ulcerative Colitis →
Gene Therapy →
Glaucoma →
Hepatology →
Hormonal Therapy →
IBS-C →
IL-23 →
Immunology →
Immunology · Biosimilar →
Immunology · JAK Inhibitor →
Infectious Disease →
JAK Inhibitor →
mCRC →
Migraine →
Monoclonal Antibody →
Multiple Myeloma →
NAFLD and Dermatology →
Neurology →
Neurology · Bipolar Disorder →
Neurology · Botulinum Toxin →
Neurology · Migraine →
Neuropsychiatry →
Not specified →
Oncology →
Oncology · B-Cell Non-Hodgkin Lymphoma →
Oncology · CLL →
Oncology · mCRC →
Ophthalmology →
Ophthalmology · Gene Therapy →
Ophthalmology · Glaucoma →
Psoriatic Arthritis →
Schizophrenia →
Ulcerative Colitis →