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Company

Bristol Myers Squibb

Pharmaceutical intelligence for Bristol Myers Squibb with 63 indexed intelligence signals across regulatory, clinical, competitive, and market developments.

Signals
27
Catalysts
36
Assets
25

Recent signals(27)

RegulatoryJuly 30, 2026

FDA Accepts Supplemental Application for REVLIMID by Bristol Myers Squibb

The FDA has accepted a supplemental application for REVLIMID (lenalidomide) submitted by Bristol Myers Squibb.

RegulatoryJuly 30, 2026

FDA Accepts Supplemental Application for POMALYST by Bristol

The FDA has accepted a supplemental application for POMALYST (pomalidomide) submitted by Bristol.

RegulatoryJuly 29, 2026

FDA Accepts Supplemental Application for REVLIMID by Bristol Myers Squibb

The FDA has accepted a supplemental application for REVLIMID (lenalidomide) from Bristol Myers Squibb.

RegulatoryJuly 24, 2026

FDA Approves Supplemental Application for INREBIC (Fedratinib Hydrochloride)

The FDA has approved a supplemental application for INREBIC, a treatment for myelofibrosis.

RegulatoryJuly 15, 2026

FDA Accepts Supplemental Application for OPDIVO QVANTIG by Bristol-Myers Squibb

The FDA has accepted a supplemental application for OPDIVO QVANTIG, which includes nivolumab and hyaluronidase-NVHY.

RegulatoryJuly 15, 2026

FDA Accepts Supplement Application for OPDIVO (Nivolumab) by Bristol Myers Squibb

The FDA has accepted a supplemental application for OPDIVO (Nivolumab) from Bristol Myers Squibb.

ClinicalJuly 14, 2026

Bristol-Myers Squibb initiates Phase 3 trial for KarXT + KarX-EC in Alzheimer's agitation

A Phase 3 study has been launched to assess the safety and efficacy of KarXT + KarX-EC for treating agitation in Alzheimer's patients.

ClinicalJuly 8, 2026

Bristol-Myers Squibb Evaluates Pomalidomide Outcomes in Relapsed/Refractory Multiple Myeloma

A retrospective study will assess clinical outcomes of pomalidomide regimens in relapsed/refractory multiple myeloma.

RegulatoryJuly 8, 2026

FDA Submission Status Update for ABANTA (Apixaban) by AZURITY

The FDA has received a submission for ABANTA (Apixaban) under NDA221024 from AZURITY, currently under standard review.

RegulatoryJuly 7, 2026

FDA Acceptance of Supplemental NDA for REVLIMID by Bristol Myers Squibb

The FDA has accepted a supplemental NDA for REVLIMID (lenalidomide) submitted by Bristol Myers Squibb.

ClinicalJuly 4, 2026

BMS initiates trial for Imzokitug in NSCLC with Pumitamig and chemotherapy

Bristol-Myers Squibb is conducting a study to evaluate Imzokitug combined with Pumitamig and PDCT in NSCLC.

ClinicalJuly 3, 2026

Bristol-Myers Squibb Compares Iberdomide to Lenalidomide in Multiple Myeloma Maintenance Therapy

A clinical trial is underway to evaluate iberdomide maintenance therapy against lenalidomide maintenance following ASCT in NDMM patients.

RegulatoryJune 30, 2026

FDA Accepts Supplemental Application for Eliquis (Apixaban)

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

ClinicalJune 29, 2026

Bristol-Myers Squibb Evaluates KarXT for Bipolar-I Disorder Manic Episodes

A clinical trial is underway to assess the efficacy and safety of KarXT in treating manic episodes of Bipolar-I Disorder.

CompetitiveJune 28, 2026

Bristol-Myers Squibb Evaluates Pumitamig vs Pembrolizumab in NSCLC Trial

A clinical trial is underway to compare the efficacy of Pumitamig and Pembrolizumab in advanced NSCLC patients with high PD-L1 expression.

ClinicalJune 28, 2026

BMS's Navlimetostat in NSCLC Trial vs. Placebo and Pembrolizumab

A clinical trial is underway to evaluate Navlimetostat combined with pembrolizumab and chemotherapy in NSCLC patients with MTAP deletion.

ClinicalJune 26, 2026

BioNTech's Pumitamig Phase III Trial in Triple-Negative Breast Cancer Underway

BioNTech SE is conducting Phase III trial of Pumitamig in combination with chemotherapy for triple-negative breast cancer.

RegulatoryJune 23, 2026

FDA Accepts Supplemental Application for YERVOY (ipilimumab)

The FDA has accepted a supplemental application for YERVOY (ipilimumab) from Bristol Myers Squibb.

RegulatoryJune 21, 2026

FDA Accepts Supplemental Application for OPDUALAG by Bristol Myers Squibb

The FDA has accepted a supplemental application for OPDUALAG, a combination of nivolumab and relatlimab-rmbw.

RegulatoryJune 20, 2026

FDA Accepts Supplement Application for YERVOY (ipilimumab)

The FDA has accepted a supplemental application for YERVOY, an immune checkpoint inhibitor.

RegulatoryJune 18, 2026

FDA Accepts Supplement Application for YERVOY (ipilimumab) by Bristol Myers Squibb

The FDA has accepted a supplemental application for YERVOY (ipilimumab) from Bristol Myers Squibb.

ClinicalJune 18, 2026

Study on Treatment Patterns for Nivolumab in Community Oncology Settings

The study will analyze treatment patterns and safety events associated with nivolumab administration routes in cancer patients.

ClinicalJune 18, 2026

Phase II Trial of Nivolumab for Persistent Cervical Cancer Shows Potential Efficacy

A phase II trial is evaluating the efficacy and side effects of nivolumab in patients with persistent, recurrent, or metastatic cervical cancer.

ClinicalJune 18, 2026

Nivolumab Phase III Trial for High Risk Stage II-IIIB Anal Cancer Initiated

A phase III trial is underway to evaluate the efficacy of nivolumab following combined modality therapy in high risk stage II-IIIB anal cancer patients.

ClinicalJune 18, 2026

Phase III Trial of Nivolumab Post-Surgery in Non-Small Cell Lung Cancer

A phase III trial is evaluating the efficacy of nivolumab following surgery and chemotherapy in patients with stage IB-IIIA non-small cell lung cancer.

ClinicalJune 17, 2026

Polyploid Giant Cancer Cells Drive Aggressiveness in Ovarian Cancer and Indicate Poor Prognosis

Polyploid giant cancer cells (PGCCs) contribute to therapy resistance and poor prognosis in ovarian cancer.

ClinicalJune 17, 2026

Lactylation-related biomarker predicts prognosis and therapy response in cutaneous melanoma

A novel lactylation-related prognostic model (CM-LP11) effectively stratifies cutaneous melanoma patients into high- and low-risk groups based on overall survival.

Upcoming catalysts

No catalysts indexed for this entity yet.

Regulatory activity(13)

RegulatoryJuly 30, 2026

FDA Accepts Supplemental Application for REVLIMID by Bristol Myers Squibb

The FDA has accepted a supplemental application for REVLIMID (lenalidomide) submitted by Bristol Myers Squibb.

RegulatoryJuly 30, 2026

FDA Accepts Supplemental Application for POMALYST by Bristol

The FDA has accepted a supplemental application for POMALYST (pomalidomide) submitted by Bristol.

RegulatoryJuly 29, 2026

FDA Accepts Supplemental Application for REVLIMID by Bristol Myers Squibb

The FDA has accepted a supplemental application for REVLIMID (lenalidomide) from Bristol Myers Squibb.

RegulatoryJuly 24, 2026

FDA Approves Supplemental Application for INREBIC (Fedratinib Hydrochloride)

The FDA has approved a supplemental application for INREBIC, a treatment for myelofibrosis.

RegulatoryJuly 15, 2026

FDA Accepts Supplemental Application for OPDIVO QVANTIG by Bristol-Myers Squibb

The FDA has accepted a supplemental application for OPDIVO QVANTIG, which includes nivolumab and hyaluronidase-NVHY.

RegulatoryJuly 15, 2026

FDA Accepts Supplement Application for OPDIVO (Nivolumab) by Bristol Myers Squibb

The FDA has accepted a supplemental application for OPDIVO (Nivolumab) from Bristol Myers Squibb.

RegulatoryJuly 8, 2026

FDA Submission Status Update for ABANTA (Apixaban) by AZURITY

The FDA has received a submission for ABANTA (Apixaban) under NDA221024 from AZURITY, currently under standard review.

RegulatoryJuly 7, 2026

FDA Acceptance of Supplemental NDA for REVLIMID by Bristol Myers Squibb

The FDA has accepted a supplemental NDA for REVLIMID (lenalidomide) submitted by Bristol Myers Squibb.

RegulatoryJune 30, 2026

FDA Accepts Supplemental Application for Eliquis (Apixaban)

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

RegulatoryJune 23, 2026

FDA Accepts Supplemental Application for YERVOY (ipilimumab)

The FDA has accepted a supplemental application for YERVOY (ipilimumab) from Bristol Myers Squibb.

RegulatoryJune 21, 2026

FDA Accepts Supplemental Application for OPDUALAG by Bristol Myers Squibb

The FDA has accepted a supplemental application for OPDUALAG, a combination of nivolumab and relatlimab-rmbw.

RegulatoryJune 20, 2026

FDA Accepts Supplement Application for YERVOY (ipilimumab)

The FDA has accepted a supplemental application for YERVOY, an immune checkpoint inhibitor.

RegulatoryJune 18, 2026

FDA Accepts Supplement Application for YERVOY (ipilimumab) by Bristol Myers Squibb

The FDA has accepted a supplemental application for YERVOY (ipilimumab) from Bristol Myers Squibb.

Clinical activity(13)

ClinicalJuly 14, 2026

Bristol-Myers Squibb initiates Phase 3 trial for KarXT + KarX-EC in Alzheimer's agitation

A Phase 3 study has been launched to assess the safety and efficacy of KarXT + KarX-EC for treating agitation in Alzheimer's patients.

ClinicalJuly 8, 2026

Bristol-Myers Squibb Evaluates Pomalidomide Outcomes in Relapsed/Refractory Multiple Myeloma

A retrospective study will assess clinical outcomes of pomalidomide regimens in relapsed/refractory multiple myeloma.

ClinicalJuly 4, 2026

BMS initiates trial for Imzokitug in NSCLC with Pumitamig and chemotherapy

Bristol-Myers Squibb is conducting a study to evaluate Imzokitug combined with Pumitamig and PDCT in NSCLC.

ClinicalJuly 3, 2026

Bristol-Myers Squibb Compares Iberdomide to Lenalidomide in Multiple Myeloma Maintenance Therapy

A clinical trial is underway to evaluate iberdomide maintenance therapy against lenalidomide maintenance following ASCT in NDMM patients.

ClinicalJune 29, 2026

Bristol-Myers Squibb Evaluates KarXT for Bipolar-I Disorder Manic Episodes

A clinical trial is underway to assess the efficacy and safety of KarXT in treating manic episodes of Bipolar-I Disorder.

ClinicalJune 28, 2026

BMS's Navlimetostat in NSCLC Trial vs. Placebo and Pembrolizumab

A clinical trial is underway to evaluate Navlimetostat combined with pembrolizumab and chemotherapy in NSCLC patients with MTAP deletion.

ClinicalJune 26, 2026

BioNTech's Pumitamig Phase III Trial in Triple-Negative Breast Cancer Underway

BioNTech SE is conducting Phase III trial of Pumitamig in combination with chemotherapy for triple-negative breast cancer.

ClinicalJune 18, 2026

Study on Treatment Patterns for Nivolumab in Community Oncology Settings

The study will analyze treatment patterns and safety events associated with nivolumab administration routes in cancer patients.

ClinicalJune 18, 2026

Phase II Trial of Nivolumab for Persistent Cervical Cancer Shows Potential Efficacy

A phase II trial is evaluating the efficacy and side effects of nivolumab in patients with persistent, recurrent, or metastatic cervical cancer.

ClinicalJune 18, 2026

Nivolumab Phase III Trial for High Risk Stage II-IIIB Anal Cancer Initiated

A phase III trial is underway to evaluate the efficacy of nivolumab following combined modality therapy in high risk stage II-IIIB anal cancer patients.

ClinicalJune 18, 2026

Phase III Trial of Nivolumab Post-Surgery in Non-Small Cell Lung Cancer

A phase III trial is evaluating the efficacy of nivolumab following surgery and chemotherapy in patients with stage IB-IIIA non-small cell lung cancer.

ClinicalJune 17, 2026

Polyploid Giant Cancer Cells Drive Aggressiveness in Ovarian Cancer and Indicate Poor Prognosis

Polyploid giant cancer cells (PGCCs) contribute to therapy resistance and poor prognosis in ovarian cancer.

ClinicalJune 17, 2026

Lactylation-related biomarker predicts prognosis and therapy response in cutaneous melanoma

A novel lactylation-related prognostic model (CM-LP11) effectively stratifies cutaneous melanoma patients into high- and low-risk groups based on overall survival.

Competitive activity(1)

CompetitiveJune 28, 2026

Bristol-Myers Squibb Evaluates Pumitamig vs Pembrolizumab in NSCLC Trial

A clinical trial is underway to compare the efficacy of Pumitamig and Pembrolizumab in advanced NSCLC patients with high PD-L1 expression.

Assets

AZURITY →
BMS-986504 →
Bristol-Myers →
cabozantinib →
Duvakitug →
Eliquis →
FDA →
Iberdomide →
Imzokitug →
INREBIC →
KEYTRUDA →
Navlimetostat →
Olaparib →
OPDIVO →
OPDIVO QVANTIG →
OPDUALAG →
Pembrolizumab →
Pomalidomide →
POMALYST →
Pumitamig →
RBMS1 →
REVLIMID →
Thalomid →
Trial Update →
YERVOY →

Therapeutic areas

Alzheimer's Disease →
Anticoagulant →
Bipolar Disorder →
Cardiovascular →
Cardiovascular · Anticoagulant →
Combination Therapy →
Gastroenterology · Ulcerative Colitis →
Hematology →
Hematology · Multiple Myeloma →
Immune Checkpoint Inhibitor →
Immunomodulator →
Immunotherapy →
Multiple Myeloma →
Myelofibrosis →
Neurology →
Neurology · Alzheimer's Disease →
Neurology · Bipolar Disorder →
Non-Small Cell Lung Cancer →
NSCLC →
Oncology →
Oncology · Combination Therapy →
Oncology · Gastric Cancer →
Oncology · Glioblastoma →
Oncology · Immune Checkpoint Inhibitor →
Oncology · Immuno-Oncology →
Oncology · Immunotherapy →
Oncology · Melanoma →
Oncology · Monoclonal Antibodies →
Oncology · Multiple Myeloma →
Oncology · Non-Small Cell Lung Cancer →
Oncology · NSCLC →
Oncology · Ovarian Cancer →
Oncology · PD-1 Inhibitor →
Oncology · Renal Cell Carcinoma →
PD-1 Inhibitor →
Triple-Negative Breast Cancer →

Indications

Alzheimer's Disease →
Bipolar Disorder →
Myelofibrosis →
Non-Small Cell Lung Cancer →
NSCLC →
Triple-Negative Breast Cancer →

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