Intelligence · Clinical Pipeline
R&D Pipeline Programs
ClinicalTrials.gov programs linked to pharma sponsors — 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 — searchable for business development and competitive intelligence.
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GSK2118436
GlaxoSmithKline
Cancer
1 trial -
GSK2585823(CLDM 1%-BPO 3% gel)
GlaxoSmithKline
Acne Vulgaris
1 trial -
GSK3196165 (Otilimab)
GlaxoSmithKline
Arthritis, Rheumatoid
1 trial -
Gemcitabine Eugia 40 mg/ml solution à diluer pour perfusion, RILVEGOSTOMIG, Cisplatine Teva 1 mg/ml solution à diluer pour perfusion.
CERO THERAPEUTICS HOLDINGS, INC.
Hihg risk of cholangiocarcinoma intra hépatic resectable
1 trial -
Givinostat 50 mg capsules, RIVAROXABAN , ACETYLSALICYLIC ACID , Givinostat 100 mg capsules, HYDROXYCARBAMIDE, ENOXAPARIN , -, Givinostat 75 mg capsules, DABIGATRAN ETEXILATE
Italfarmaco S.p.A.
JAK2V617F-positive high-risk Polycythemia Vera
1 trial -
Grafalon 20 mg/ml concentrato per soluzione per infusione
The George Institute
To analyze whether the anti-rejection treatment of borderline lesions can modify the expression and klotho levels, as well as proinflammatory cytokines that regulate klotho expression at both years post-transplant., Know in a controlled and randomized clinical trial, carried out in low-risk patients immunological and stable renal function, if the treatment of BL lesions, detected in the third month post-transplant, with rabbit polyclonal antilymphocytic globulin prevents or slows the progression of chronic histological lesions of the graft (FIAT) and the deterioration of its function compared to clinical follow-up conventional, after two years of post-transplant follow-up.
1 trial -
HEPARIN , NADROPARIN
Disc Medicine
All patients who receive ECMO treatment during the study period in one the participating centers from which (deferred) informed consent is obtained. Patients in whom the ECMO is only used to bridge a procedure like a high risk percutaneous coronary intervention or during surgery are excluded.
1 trial -
HVA
The First People's Hospital of Lianyungang
Newly Diagnosed Acute Myeloid Leukemia With High Risk
1 trial -
IMBRUVICA 140 mg hard capsules, Calquence 100 mg film-coated tablets, Calquence 100 mg hard capsules, IMBRUVICA 140 mg hard capsules
Lacuna Pharma Pty Ltd
High Risk Chronic Lymphocytic Leukaemia
1 trial -
INEBILIZUMAB, 10 mL (nominal) solution containing 10 mM histidine/histidine hydrochloride, 75 mM sodium chloride, 106 mM (4% [w/v]) trehalose dihydrate, and 0.02% (w/v) polysorbate 80, pH 6.0
Elan Pharma International
Myasthenia Gravis which is either due to acetylcholine receptor antibodies (AChR) or muscle specific kinase antibodies (MuSK).
1 trial -
InfectoScab® 5 % Crème, Permethrin, DRIPONIN 3 mg Tabletten
Alphapharm Pty Ltd
Scabies
1 trial -
Influenza vaccine GSK1562902A Formulation 1
GlaxoSmithKline
Influenza
1 trial -
Influenza vaccine GSK2321138A
GlaxoSmithKline
Influenza
1 trial -
Insulin degludec/insulin aspart
Novo Nordisk A/S
Diabetes
1 trial -
Insulin icodec
Novo Nordisk A/S
Diabetes, Type 2
1 trial -
JEVTANA 60 mg concentrate and solvent for solution for infusion.
Ningbo Cancer Hospital
Patients with localized prostate cancer and high-risk features of relapse.
1 trial -
JNJ-42756493, GEMCITABINE , MITOMYCIN
Janssen-Cilag International N.V.
FGFR+ Intermediate-risk Non-muscle Invasive Bladder Cancer
1 trial -
JNJ-56021927
Ningbo Cancer Hospital
High-risk biochemically-relapsed prostate adenocarcinoma following radical prostatectomy.
1 trial -
KEYTRUDA 25 mg/mL concentrate for solution for infusion
Ningbo Cancer Hospital
High risk resected melanoma.
1 trial -
KEYTRUDA 25 mg/mL concentrate for solution for infusion, ADSTILADRIN, GEMCITABINE , DOCETAXEL
Ferring Pharmaceuticals
High-risk Bacillus Calmette-Guerin (BCG)-unresponsive non-muscle-invasive bladder cancer (NMIBC) with carcinoma in situ(CIS) with or without papillary tumours
1 trial -
LETROZOLE, DOCETAXEL, ANASTROZOLE, LEUPRORELIN ACETATE, LEUPRORELIN ACETATE, TAMOXIFEN, EPIRUBICIN, DOXORUBICIN, GOSERELIN, TRIPTORELIN, EXEMESTANE, PACLITAXEL, CYCLOPHOSPHAMIDE, GOSERELIN, TRIPTORELIN
Ningbo Cancer Hospital
Premenopausal patients with high-risk HR-positive/HER2-negative breast cancer (BC) defined by tumour size and axillary lymph node status. One of the following must apply: a. 1-3 lymph nodes involved AND any invasive tumour size. b. node negative (including micrometastases in at least 1 node [i.e. deposit >0.2-2mm diameter]) AND invasive tumour size ≥ 50mm.
1 trial -
LETROZOLE, ELACESTRANT, ANASTROZOLE, EXEMESTANE, TAMOXIFEN, ELACESTRANT
Stemline Therapeutics B.V.
Node-positive, Estrogen Receptor-positive, HER2-negative, Early Breast Cancer with High Risk of Recurrence
1 trial -
LGP PURE CBD 200, caprylic/capric triglyceride liquid
The George Institute
Patients with stage I, II, III hormone-receptor positive (HR+) breast cancer (BC) receiving adjuvant aromatase inhibitors (AI) and presenting AI-related musculoskeletal pain (reported average joint pain score of ≥ 4 out of 10 on the Brief Pain Inventory)
1 trial -
LGP PURE CBD 200, caprylic/capric triglyceride liquid
The George Institute
Patients with stage I, II, III hormone-receptor positive (HR+) breast cancer (BC) receiving adjuvant aromatase inhibitors (AI) and presenting AI-related musculoskeletal pain (reported average joint pain score of ≥ 4 out of 10 on the Brief Pain Inventory)
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 1–3), 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 — 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