New drug approvals - December 2025

 

  • Please click here for a list of summary reports of benefit-risk assessments.
  • Please click here for description of application types.

For the most updated information including approved indication/s related to registered therapeutic products, please refer to the Register of Therapeutic Products.

Product NameBILAXTEN ORODISPERSIBLE TABLET 20 MG
Active Ingredient (Strength) BILASTINE(20 MG)
Application type NDA-2
Product Registrant A. MENARINI SINGAPORE PTE. LTD.
Date of Approval 02/12/2025
Registration No. SIN17410P
Indications:
Symptomatic treatment of allergic rhino-conjunctivitis and urticaria. BILAXTEN is indicated in adults and adolescents (12 years of age and over).

 

Product NameHYRIMOZ SOLUTION FOR INJECTION IN PRE-FILLED PEN 40MG/0.4ML,
HYRIMOZ SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE 40MG/0.4ML,
HYRIMOZ SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE 20MG/0.2ML
Active Ingredient (Strength) Adalimumab(40 mg /0.4 ml),
Adalimumab(40 mg /0.4ml),
Adalimumab(20 mg /0.2 ml)
Application type NDA-2: Biosimilar
Product Registrant SANDOZ SINGAPORE PTE. LTD.
Date of Approval 11/12/2025
Registration No. SIN17412P,
SIN17413P,
SIN17414P
Indications:
ADULTS
Rheumatoid Arthritis
Hyrimoz is indicated for reducing signs and symptoms and inhibiting the progression of structural damage and improving physical function in adult patients with moderately to severely active rheumatoid arthritis who have had an inadequate response to one or more DMARDs.

Hyrimoz can be used alone or in combination with methotrexate or other DMARDs.

Hyrimoz, in combination with MTX, can also be used in the treatment of patients with recently diagnosed moderate to severely active rheumatoid arthritis who have not received methotrexate.

Psoriatic Arthritis
Hyrimoz is indicated for reducing signs and symptoms of active arthritis in adult patients with moderate to severe psoriatic arthritis when the response to previous DMARD therapy has been inadequate. Adalimumab has been shown to reduce the rate of progression of peripheral joint damage as measured by X-ray in patients with polyarticular symmetrical subtypes of the disease and to improve physical function.

Hyrimoz can be used alone or in combination with DMARDs.

Ankylosing Spondylitis
Hyrimoz is indicated for reducing signs and symptoms in adult patients with active ankylosing spondylitis who have had an inadequate response to conventional therapy.

Crohn’s Disease
Hyrimoz is indicated for the treatment of moderate to severe active Crohn’s disease in adults to reduce the signs and symptoms of the disease and to induce and maintain clinical remission in patients who have had an inadequate response to conventional therapies, or who have lost response to or are intolerant of infliximab. For induction treatment, Hyrimoz should be given in combination with corticosteroids. Hyrimoz can be given as monotherapy in case of intolerance to corticosteroids or when continued treatment with corticosteroids is inadequate.

Ulcerative Colitis
Hyrimoz is indicated for treatment of moderately to severely active ulcerative colitis in adult patients who have had an inadequate response to conventional therapy including corticosteroids and/or 6-mercaptopurine (6-MP) or azathioprine (AZA), or who are intolerant to or have medical contraindications for such therapies.

Plaque Psoriasis
Hyrimoz is indicated for the treatment of adult patients with moderate to severe chronic plaque psoriasis who are candidates for systemic therapy or phototherapy and when other systemic therapies are medically less appropriate.

Hidradenitis Suppurativa
Hyrimoz is indicated for the treatment of active moderate to severe hidradenitis suppurativa (acne inversa) in adult patients with an inadequate response to conventional systemic HS therapy.

Uveitis
Hyrimoz is indicated for the treatment of non-infectious intermediate, posterior and panuveitis in adult patients who have had an inadequate response to corticosteroids, in patients in need of corticosteroid-sparing, or in whom corticosteroid treatment is inappropriate.

PEDIATRICS
Juvenile Idiopathic Arthritis

Polyarticular Juvenile Idiopathic Arthritis
Hyrimoz in combination with methotrexate is indicated for the treatment of active polyarticular juvenile idiopathic arthritis (pJIA), in patients 2 years of age and older, who have had an inadequate response to one or more disease-modifying anti-rheumatic drugs (DMARDS).

Hyrimoz can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate (for the efficacy in monotherapy see Clinical Efficacy and Safety). Adalimumab has not been studied in patients aged less than 2 years.

Enthesitis-Related Arthritis
Hyrimoz is indicated for the treatment of active enthesitis-related arthritis in patients, 6 years of age and older, who have had an inadequate response to, or who are intolerant of, conventional therapy.

Pediatric Crohn's Disease
Hyrimoz is indicated for reducing signs and symptoms and inducing and maintaining clinical remission in pediatric patients, 6 years of age and older, with moderately to severely active Crohn’s disease who have had an inadequate response to conventional therapy.

Pediatric Plaque Psoriasis
Hyrimoz is indicated for the treatment of severe chronic plaque psoriasis in children and adolescents from 4 years of age who have had an inadequate response to or are inappropriate candidates for topical therapy and phototherapy.

Adolescent Hidradenitis Suppurativa
Hyrimoz is indicated for the treatment of active moderate to severe hidradenitis suppurativa (acne inversa) in adolescents from 12 years of age with an inadequate response to conventional systemic hidradenitis suppurativa (HS) therapy.

Pediatric Uveitis
Hyrimoz is indicated for the treatment of chronic non-infectious anterior uveitis in pediatric patients 2 years of age and older who have had an inadequate response to or are intolerant to conventional therapy, or in whom conventional therapy is inappropriate.

Pediatric Ulcerative Colitis

Hyrimoz is indicated for inducing and maintaining clinical remission in pediatric patients 5 years of age or older with moderately to severely active ulcerative colitis who have had an inadequate response to conventional therapy including corticosteroids and/or 6-mercaptopurine (6-MP) or azathioprine (AZA), or who are intolerant to or have medical contraindications for such therapies.

 

Product NameK-CAB FILM-COATED TABLETS 25MG
Active Ingredient (Strength) Tegoprazan(25mg)
Application type NDA-2
Product Registrant UNITED ITALIAN TRADING CORPORATION (PRIVATE) LIMITED
Date of Approval 03/12/2025
Registration No. SIN17411P
Indications:
K-CAB is indicated for the treatment of Erosive Gastroesophageal Reflux Diseases, Non-Erosive Gastroesophageal Reflux Disease and Gastric Ulcer.
K-CAB is also indicated for the eradication of H. pylori when concurrently given with appropriate antibiotic therapy treatment in patients with peptic ulcer and/or chronic atrophic gastritis.
K-CAB is indicated for maintenance treatment to prevent the recurrence of Erosive Gastroesophageal Reflux Disease.

 

Product NameMITOCIN POWDER FOR SOLUTION FOR INJECTION 10 MG/VIAL
Active Ingredient (Strength) Mitomycin(10mg/vial)
Application type NDA-1
Product Registrant ALLIANCE PHARM PTE. LTD.
Date of Approval 29/12/2025
Registration No. SIN17419P
Indications:
Intravesical use for recurrence prevention in low grade bladder cancer after transurethral resection.

 

Product NameVAZKEPA SOFT CAPSULES 998MG
Active Ingredient (Strength) Icosapent ethyl(998 mg)
Application type NDA-2
Product Registrant LOTUS INTERNATIONAL PTE. LTD.
Date of Approval 12/12/2025
Registration No. SIN17418P
Indications:
VAZKEPA (icosapent ethyl) is indicated as an adjunct to maximally tolerated statin therapy to reduce the risk of cardiovascular events in adult patients with elevated triglyceride levels (≥1.7mmol/L) and
∙ established cardiovascular disease or
∙ diabetes mellitus and at least 2 or more additional risk factors for cardiovascular disease.

 

Product NameZEYZELF® TWICE WEEKLY TRANSDERMAL PATCH 4.6MG/24H,
ZEYZELF® TWICE WEEKLY TRANSDERMAL PATCH 9.5MG/24H
Active Ingredient (Strength) Rivastigmine(25.92mg),
Rivastigmine(51.84mg)
Application type NDA-2,
NDA-3
Product Registrant LUYE PHARMA (SINGAPORE) PTE. LTD.
Date of Approval 12/12/2025
Registration No. SIN17415P,
SIN17416P
Indications:
Symptomatic treatment of mild to moderately severe Alzheimer’s dementia.

 

 

Healthcare professional, Industry member, Therapeutic Products
Published:

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New Drug Approvals

2 Feb 2026