Intelligence Β· Clinical Pipeline
R&D Pipeline Programs
ClinicalTrials.gov programs linked to pharma sponsors β phase, modality, and trial IDs for BD and competitive intelligence.
- Programs indexed
- 20,548
- Companies
- 1,769
- Drugs tracked
- 4,797
Quick answer
NovaPharmaNews tracks 20,548 pharmaceutical R&D pipeline programs sourced from ClinicalTrials.gov, linked to sponsor companies. Each profile includes development phase, modality, trial status, NCT identifiers, and indication text β searchable for business development and competitive intelligence.
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Treatment as Usual
Camp4 Therapeutics Corp
Post-Traumatic Stress Disorder
1 trial -
Tumour heterogeneity studies based on dedicated breast PET using proliferation radiotracers: early detection of the treatment response.
The George Institute
Breast cancer
1 trial -
VLY-686
Vanda Pharmaceuticals Netherlands B.V.
Treatment-resistant Pruritus Associated With Atopic Dermatitis
1 trial -
Vancomycin Pre-Treatment
Seres Therapeutics
Ulcerative Colitis
1 trial -
Venclyxto 100 mg film-coated tablets, RITUXIMAB, Calquence 100 mg film-coated tablets, Venclyxto 50 mg film-coated tablets, RITUXIMAB, Venclyxto 10 mg film-coated tablets
AstraZeneca AB
Treatment NaΓ―ve Mantle Cell Lymphoma
1 trial -
X-vivo 15 (serum-free growth medium manufactured under gmp and commercially available from Lonza)
Biogen
Peripherial arterial disease (PAD) & Chronic-Limb Threatening Ischemia (CLTI) patients who have not responded to standard pharmacological treatment or control of risk factors, and/or had a revascularisation with continued presence of smaller vessel (microvasculature) disease, and do not have the option of a revascularization treatment.
1 trial -
YTB323, Flebogamma DIF 50 mg/ml solution for infusion, TOCILIZUMAB, FLUDARABINE PHOSPHATE, CYCLOPHOSPHAMIDE
Novartis Pharmaceuticals
Treatment-resistant generalized Myasthenia Gravis
1 trial -
Zelboraf 240 mg film-coated tablets
Ningbo Cancer Hospital
Patients with metastatic or unresectable locally advanced malignancies harboring BRAF genomic alterations, the biological target of vemurafenib, and who are no more amenable to curative treatment
1 trial -
conventional therapy plus low dose hUC-MSCs treatment
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Liver Cirrhosis
1 trial -
idecabtagene vicleucel
Celgene Europe Limited
Relapsed and refractory multiple myeloma (RRMM), multiple myeloma (MM) with progression within 18 months of initial treatment/ or newly diagnosed multiple myeloma (NDMM) with suboptimal response post autologous stem cell transplant (ASCT) (Cohort 3 only)
1 trial -
long course radiotherapy + capecitabine + PD-1 monoclonal antibody treatment combinations
BEONE MEDICINES AUS PTY LTD
Colorectal Neoplasms
1 trial -
rituximab /Dexamethasone/cyclophosphamide
The First People's Hospital of Lianyungang
Treatment
1 trial -
"A study in healthy people to test how 2 different formulations of a combination treatment (vicadrostat and empagliflozin) are taken up in the body and how food influences the amount of the medicines in the blood"
Boehringer Ingelheim
Healthy volunteer trial
1 trial -
610
Sunshine Guojian Pharmaceutical (Shanghai) Co.,
add-on Maintenance Treatment of Patients With Severe Eosinophilic Asthma
1 trial -
90 mg dose of the hydrocodone bitartrate extended-release tablet administered as either two 45-mg tablets (Treatment A) or one 90-mg tablet (Treatment B).
Teva Pharma GmbH
Pain
1 trial -
A First In Human Phase I Trial Evaluating safety, tolErability and ResponSe of [211At]At-Girentuximab (ATO-101β’) in PatiEnts with Non-Muscle-InVasive BladdER CANCEr Refractory to Standard Treatment (PERSEVERANCE EU)
CERO THERAPEUTICS HOLDINGS, INC.
Non-Muscle-Invasive Bladder Cancer (NMIBC) refractory
1 trial -
A PHASE 1, OPEN-LABEL, DOSE ESCALATION AND DOSE EXPANSION STUDY OF CLN-049 FOR THE TREATMENT OF ACUTE MYELOID LEUKEMIA (AML) PATIENTS WITH MEASURABLE RESIDUAL DISEASE (MRD)
Cullinan Therapeutics
Acute Myeloid Leukemia (AML) with Measurable Residual Disease (MRD)
1 trial -
A Phase 1 study to test for safety and activity of an oral investigational drug, in patients with AML or other blood or bone marrow malignacies with an IDH1 mutation.
The George Institute
AG-120 is being investigated for the treatment of patients with advanced hematologic malignancies that are IDH1 mutation.
1 trial -
A Phase 1 study to test the safety of an oral investigational drug (either AG-120 or AG-221) in combination with standard chemotherapeutic treatment for patients newly diagnosed with a blood malignancy (AML) with an IDH1 mutation and/or IDH2 mutation
The George Institute
Newly Diagnosed Acute Myeloid Leukemia with an IDH1 and/or IDH2 Mutation
1 trial -
A Phase 1, Open-Label, Safety and Tolerability Study of INCB057643 in Participants With Myelofibrosis and Other Advanced Myeloid Neoplasms
Incyte
Treatment of participants with MF, MDS, ET, or MDS/MPN
1 trial -
A Phase 1a/1b Study of ELVN-001 for the Treatment of Chronic Myeloid Leukemia
Enliven Therapeutics
Chronic myeloid leukemia
1 trial -
A Phase 1b Study of AMG 757 in Subjects with Neuroendocrine Prostate Cancer
Amgen
Adult subjects with de novo or treatment-emergent neuroendocrine prostate cancer
1 trial -
A Phase 1b Study of Bispecific T Cell Redirection Antibodies in Combination with Checkpoint Inhibition for the Treatment of Participants with Relapsed or Refractory Multiple Myeloma
Janssen-Cilag International N.V.
Relapsed or Refractory Multiple Myeloma
1 trial -
A Phase 1b Study of Subcutaneous Daratumumab Regimens in Combination with Bispecific T Cell Redirection Antibodies for the Treatment of Subjects with Multiple Myeloma
Janssen-Cilag International N.V.
Multiple myeloma
1 trial
Frequently asked questions
What is the NovaPharmaNews pipeline directory?
It is a searchable index of 20,548 clinical development programs grouped by sponsor company, with phase (Phase 1β3), modality, trial status, and linked NCT IDs from ClinicalTrials.gov.
Where does pipeline data come from?
Program records are derived from ClinicalTrials.gov and linked to NovaPharmaNews company profiles. Trial status and phase reflect registry data at last sync β verify on ClinicalTrials.gov before investment or partnering decisions. See our data sources page for attribution.
How do I find pipeline programs by company or phase?
Use the search box to match program name, indication, company name, or slug. Results are ordered with late-stage (Phase 3) programs first. Open any row to view the full program profile under its sponsor company.
Data attribution and licensing: Data sources