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.
-
Anifrolumab, Anifrolumab Placebo
AstraZeneca AB
Polymyositis or dermatomyositis according to 2017 EULAR / ACR classification criteria
1 trial -
BAY 1841788, TRIPTORELIN
Ningbo Cancer Hospital
Patients with localised prostate cancer and high-risk features of relapse (minimum 2 high-risk criteria from National Comprehensive Cancer Network (NCCN) classification)1 and with no detectable metastasis, including no evidence of pelvic lymph node metastasis on next-generation imaging (PSMA PET/CT).
1 trial -
Garetosmab
Regeneron UK Limited
Fibrodysplasia Ossificans Progressiva
1 trial -
KEYTRUDA 25 mg/mL concentrate for solution for infusion, Saline Solution
Merck Sharp and Dohme
Stage III melanoma (AJCC R0) with histologically confirmed cutaneous melanoma metastatic to lymph node, classified as (AJCC, 2010): Stage IIIA with metastasis > 1 mm; any Stage IIIB or IIIC (no in-transit metastases)
1 trial -
Ozempic 1 mg solution for injection in pre-filled pen, Semaglutide placebo, solution for injection in 1.5 mL pre-filled PDS290 pen injector
NovoThirteen
While it is well-established that long-term good glycaemic control will reduce the risk of diabetic retinopathy development and progression, intensification of glycaemic control has also been associated with an initial worsening of diabetic retinopathy. This phenomenon is known as βearly worseningβ. The rationale of this trial is to establish the long-term effects of semaglutide on diabetic retinopathy in subjects with type 2 diabetes (T2D) using validated and standardised ophthalmic assessments. This trial is a post-authorisation safety study (PASS) conducted as a commitment to the European Medicines Agency
1 trial -
Placebo matching to garetosmab, Garetosmab
Lacuna Pharma Pty Ltd
Fibrodysplasia Ossificans Progressiva
1 trial -
Privigen 100 mg/ml solution for infusion, Gammanorm, 165 mg/ml, oplossing voor injectie, Octagam 10%, oplossing voor infusie, Nanogam 100 mg/ml oplossing voor infusie, Hizentra 200 mg/ml solution for subcutaneous injection, HyQvia 100 mg/ml solution for infusion for subcutaneous use, Cuvitru 200 mg/ml oplossing voor subcutane injectie, KIOVIG 100 mg/ml solution for infusion, CUTAQUIG 165 mg/mL, solution injectable, GAMMAGARD S/D 5,0 g, poeder en oplosmiddel voor oplossing voor infusie.
Disc Medicine
Primary antibody deficiency: - Unclassified antibody deficiency (unPAD) - IgA deficiency - Specific polysaccharide antibody deficiency (SPAD) - IgG subclass deficiency (IgSD) - Common variable immunodeficiency (CVID) - Agammaglobulinemia (X-linked or otherwise)
1 trial -
Solution de chlorure de sodium Γ 0,9%, Allogeneic umbilical cord derived MSC (thawed and washed)
Pari Pharma GmbH
Adult Patients kidney transplant recipients who have developed chronic humoral rejection, diagnosed through a kidney biopsy (Banff 2017 Classification), resistant to conventional treatment (3 injections at one-month intervals of 2g/kg of IVIG)
1 trial -
garetosmab
Regeneron UK Limited
Fibrodyplasia Ossificans Progressiva (FOP)
1 trial -
garetosmab
Regeneron UK Limited
Fibrodysplasia Ossificans Progressiva (FOP)
1 trial -
INCB000928, Placebo
Incyte
Fibrodysplasia Ossificans Progressiva
1 trial -
Placebo capsule
Ipsen
Fibrodysplasia Ossificans Progressiva
1 trial -
REGN2477
Regeneron UK Limited
Fibrodysplasia Ossificans Progressiva
1 trial -
TOCILIZUMAB , SECUKINUMAB , ANAKINRA , ADALIMUMAB , RITUXIMAB, USTEKINUMAB
Pari Pharma GmbH
Patients displaying a non-classified, severe and resistant inflammatory disease
1 trial -
Yondelis 1 mg powder for concentrate for solution for infusion, DOXORUBICINE ARROW 2 mg/ml, solution pour perfusion
Ningbo Cancer Hospital
Localized, resected, FIGO stage I (2018 classification), uterine leiomyosarcoma
1 trial -
Assessment of narrowing of blood vessels after single application of two clascoterone formulations (cream and solution) onto the skin in comparison to three marketed topical corticosteroids
Cassiopea S.p.A.
Test of vasocontriction properties for classification of topical steroid potency
1 trial -
phacoemulsification
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Astigmatism
1 trial -
5-gene classification model
Hospital Authority, Hong Kong
ABO Blood Type Incompatible Kidney Transplantation
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