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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AG-120/S95031 250mg film-coated tablet, Ivosidenib-matched Placebo Tablets
The George Institute
Locally advanced or metastatic conventional chondrosarcoma with an IDH1 mutation, untreated or previously treated with 1 or 2 systemic treatment regimens
1 trial -
Conventional medical treatment
Lxo Ireland Designated Activity Company
Coronary Atherosclerosis and Other Heart Disease
1 trial -
Conventional sound generator (SG)
Camp4 Therapeutics Corp
Subjective Tinnitus
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 -
Solution de chlorure de sodium à 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 -
XEOMIN 200 unités, poudre pour solution injectable, Placebo of Xeomin 200 U
Pari Pharma GmbH
Adult patients with indication for conventional cardiac surgery (CABG, aortic replacement, or ascending aorta surgery)
1 trial -
A Phase I/II open label study to assess safety and preliminary evidence of a therapeutic effect of Azeliragon combined with conventional concurrent radiation and temozolomide in patients with newly diagnosed glioblastoma.
Lacuna Pharma Pty Ltd
Glioblastoma
1 trial -
ACETYLCYSTEINE , DEXAMETHASONE , DIPHENHYDRAMINE , GLUCOSE
Inhibrx Biosciences
Unresectable or metastatic conventional chondrosarcoma
1 trial -
Anterior lamellar nanostructured artificial human cornea.
Lxo Ireland Designated Activity Company
Severe Trophic Corneal Ulcers Refractory to Conventional Treatment
1 trial -
CASPONEB - Phase II safety lead-in randomized blind placebo controlled clinical trial : efficacy and safety of caspofungin aerosols for the curative treatment of Pneumocystis pneumonia in adjunction of conventional systemic antifungal therapy
Tour Hekla
Pneumocystis pneumonia
1 trial -
Conventional Roux-en-Y Gastrojejunostomy
The First People's Hospital of Lianyungang
Gastric Cancer
1 trial -
Conventional therapy
Chinese Academy of Sciences
Decompensated Cirrhosis
1 trial -
Conventional treatment plus intravenous infusion of allogenic mesenchymal stem cells from adipose tissue.
Lxo Ireland Designated Activity Company
Graft Versus Host Disease
1 trial -
INBRX-109
Inhibrx Biosciences
Conventional Chondrosarcoma
1 trial -
conventional therapy plus low dose hUC-MSCs treatment
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Liver Cirrhosis
1 trial -
A dose-finding Phase I study of F8IL10 intra-articular treatment in Rheumatoid Arthritis
Philogen S.p.A.
Patients with Rheumatoid Arthritis (RA) who, despite treatment with stable doses (for at least 3 months) of disease-modifying antirheumatic drugs (DMARDs, conventional, biologic and/or targeted synthetic), present arthritis flare(s) suitable for intra-articular (IA) injection in a knee, shoulder, ankle, wrist or elbow.
1 trial -
AN OPEN-LABEL, RANDOMIZED, SINGLE DOSE, TWO-STAGE CROSSOVER ADAPTIVE BIOEQUIVALENCE STUDY OF TRIAMCINOLONE ACETONIDE 40 MG/ML STERILE INJECTABLE SUSPENSION (Test product–Lisapharma S.p.A) VERSUS KENACORT® 40 MG/ML SUSPENSION (Reference product – Bristol Myers Squibb) AFTER INTRAMUSCULAR ADMINISTRATION TO HEALTHY VOLUNTEERS
Lacuna Pharma Pty Ltd
Intramuscular administration of triamcinolone acetonide Lisapharma (Injectable suspension of triamcinolone acetonide) is indicated for systemic corticosteroid therapy in morbid conditions such as allergic syndrome (to control severe or debilitating conditions not treatable in a conventional way), dermatoses, generalized rheumatoid arthritis and other connective tissue diseases.
1 trial -
clinical trial to determine the feasibility and safety of the mesenchymal stem cells use in women over 50 years of age with urinary incontinencee
The George Institute
Stress or mixed urinary incontinence in women over 50 years of age not responding to conventional treatments
1 trial -
Conventional therapy + S (+)-Ketamine
Xiyuan Hospital of China Academy of Chinese Medical Sciences
S-ketamine
1 trial -
conventional dose epinephrine
Hospital Authority, Hong Kong
Croup
1 trial -
Combination Product: Conventional third-line therapy
The First People's Hospital of Lianyungang
Colorectal Cancer (CRC)
1 trial -
Conventional Artificial Cycle Therapy
Jian Li
Infertility, Female
1 trial -
Conventional second-line therapy
The First People's Hospital of Lianyungang
Colorectal Cancer (CRC)
1 trial -
Conventional third-line therapy
The First People's Hospital of Lianyungang
Colorectal Cancer (CRC)
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