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Company

Sanofi

Pharmaceutical intelligence for Sanofi with 18 indexed intelligence signals across regulatory, clinical, competitive, and market developments.

Signals
11
Catalysts
7
Assets
8

Recent signals(11)

RegulatoryJuly 30, 2026

FDA Accepts Supplemental Application for AVAPRO by Sanofi

The FDA has accepted a supplemental application for AVAPRO (irbesartan) from Sanofi.

RegulatoryJuly 29, 2026

FDA Accepts Supplemental NDA for AVAPRO by Sanofi

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

ClinicalJuly 26, 2026

Isatuximab Evaluated in Stem Cell Transplant for Multiple Myeloma and Lymphoma

A clinical trial is investigating the effects of Isatuximab on the immune system during stem cell recovery in multiple myeloma and lymphoma patients.

Upcoming catalysts

No catalysts indexed for this entity yet.

Regulatory activity(5)

RegulatoryJuly 30, 2026

FDA Accepts Supplemental Application for AVAPRO by Sanofi

The FDA has accepted a supplemental application for AVAPRO (irbesartan) from Sanofi.

RegulatoryJuly 29, 2026

FDA Accepts Supplemental NDA for AVAPRO by Sanofi

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

RegulatoryJuly 15, 2026

FDA Accepts Application for SARCLISA (Isatuximab-IRFC) by Sanofi

The FDA has accepted the Biologics License Application for SARCLISA (Isatuximab-IRFC) from Sanofi.

Clinical activity(5)

ClinicalJuly 26, 2026

Isatuximab Evaluated in Stem Cell Transplant for Multiple Myeloma and Lymphoma

A clinical trial is investigating the effects of Isatuximab on the immune system during stem cell recovery in multiple myeloma and lymphoma patients.

ClinicalJuly 23, 2026

Trial to Assess Recruitment Methods for Type 1 Diabetes Screening

A clinical trial is evaluating the effectiveness of different recruitment communication methods for type 1 diabetes screening.

ClinicalJune 25, 2026

Sanofi's Venglustat Phase 3 Trial Targets Left Ventricular Mass in Fabry Disease

Sanofi is conducting Phase 3 trial to assess the efficacy of venglustat on left ventricular mass index in Fabry disease patients.

Competitive activity

No signals indexed for this entity yet.

Assets

AVAPRO →
Dupixent →
Isatuximab →
Itepekimab →
Nirsevimab →
SARCLISA →
Tolebrutinib →
Venglustat →

Therapeutic areas

Antihypertensive →
Cardiology →
Cardiology · Fabry Disease →
Cardiovascular →
Chronic Rhinosinusitis with Nasal Polyps →
Dermatology · Atopic Dermatitis →
Endocrinology →
Fabry Disease →
Hematology →
Immunology · IL-4/IL-13 →
Infectious Disease →
Infectious Disease · Respiratory Syncytial Virus (RSV) →

Indications

Fabry Disease →
Infectious Disease →
Multiple sclerosis →
T-cell Acute Lymphoblastic Leukemia →
Type 1 Diabetes →

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ClinicalJuly 23, 2026

Trial to Assess Recruitment Methods for Type 1 Diabetes Screening

A clinical trial is evaluating the effectiveness of different recruitment communication methods for type 1 diabetes screening.

RegulatoryJuly 15, 2026

FDA Accepts Application for SARCLISA (Isatuximab-IRFC) by Sanofi

The FDA has accepted the Biologics License Application for SARCLISA (Isatuximab-IRFC) from Sanofi.

RegulatoryJuly 3, 2026

FDA Approves Supplemental Application for SARCLISA (Isatuximab-IRFC)

The FDA has approved a supplemental application for SARCLISA, a monoclonal antibody targeting CD38.

RegulatoryJuly 1, 2026

FDA Accepts Supplement for SARCLISA (Isatuximab-IRFC) by Sanofi

The FDA has accepted a supplemental application for SARCLISA, a monoclonal antibody targeting CD38.

ClinicalJune 25, 2026

Sanofi's Venglustat Phase 3 Trial Targets Left Ventricular Mass in Fabry Disease

Sanofi is conducting Phase 3 trial to assess the efficacy of venglustat on left ventricular mass index in Fabry disease patients.

StrategyJune 24, 2026

Sanofi's Nirsevimab Study to Assess RSV Immunisation Rates in Queensland Infants

A study sponsored by Sanofi aims to determine nirsevimab immunisation rates among infants in Queensland during the RSV season.

ClinicalJune 23, 2026

Sanofi and Regeneron Launch Phase 3 Study on Itepekimab for Chronic Rhinosinusitis

A Phase 3 extension study has been initiated to assess the long-term safety and tolerability of itepekimab in adults with inadequately controlled chronic rhinosinusitis with nasal polyps.

ClinicalJune 22, 2026

Isatuximab Trial for Relapsed/Refractory CD38 Positive T-ALL Initiated

A new trial is evaluating Isatuximab in adult patients with relapsed/refractory CD38 positive T-cell acute lymphoblastic leukemia, focusing on two treatment cohorts.

Regulatory
July 3, 2026

FDA Approves Supplemental Application for SARCLISA (Isatuximab-IRFC)

The FDA has approved a supplemental application for SARCLISA, a monoclonal antibody targeting CD38.

RegulatoryJuly 1, 2026

FDA Accepts Supplement for SARCLISA (Isatuximab-IRFC) by Sanofi

The FDA has accepted a supplemental application for SARCLISA, a monoclonal antibody targeting CD38.

ClinicalJune 23, 2026

Sanofi and Regeneron Launch Phase 3 Study on Itepekimab for Chronic Rhinosinusitis

A Phase 3 extension study has been initiated to assess the long-term safety and tolerability of itepekimab in adults with inadequately controlled chronic rhinosinusitis with nasal polyps.

ClinicalJune 22, 2026

Isatuximab Trial for Relapsed/Refractory CD38 Positive T-ALL Initiated

A new trial is evaluating Isatuximab in adult patients with relapsed/refractory CD38 positive T-cell acute lymphoblastic leukemia, focusing on two treatment cohorts.

Monoclonal Antibody →
Multiple Myeloma →
Neurology →
Oncology →
Oncology · T-cell Acute Lymphoblastic Leukemia →
Otolaryngology →
Otolaryngology · Chronic Rhinosinusitis with Nasal Polyps →
Respiratory Syncytial Virus (RSV) →
T-cell Acute Lymphoblastic Leukemia →
Type 1 Diabetes →