VetSheet

Rabacfosadine

Also known as: Tanovea-CA1 · GS-9219 · VDC-1101

Reviewed by the VetSheet Veterinary TeamUpdated Apr 5, 2026Evidence-based veterinary reference

0.82-1 mg/kgIV· once every 21 days· over 30 min
🐕

Doses are a clinical reference for licensed veterinary professionals. Always confirm against the current label and the individual patient.

Dosing by species

🌎 NA — North America🌍 EU — Europe

Dogs

IndicationDoseRouteFrequencyDurationRegion
Lymphoma (B and T cell) and multiple myeloma0.82-1 mg/kgIVonce every 21 daysover 30 min🌍 EU
  • Lymphoma (B and T cell) and multiple myeloma: Has been used in combination with doxorubicin at weeks 0, 6, 12 as part of an alternating protocol.

Doses are a clinical reference for licensed veterinary professionals. Always confirm against the current label and the individual patient.

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Overview

Rabacfosadine is a novel antineoplastic agent used primarily in veterinary medicine for the treatment of canine lymphoma (both B-cell and T-cell) and multiple myeloma.

​Clinical Warning:​ This is a potent cytotoxic drug. It must only be prepared and administered by trained personnel following strict chemotherapeutic safety guidelines.

Mechanism of action

Rabacfosadine is a prodrug of the nucleotide analogue PMEG (9-(2-phosphonylmethoxyethyl)guanine). Once converted, it acts by inhibiting DNA polymerases → preventing DNA synthesis → causing cytotoxicity and apoptosis in rapidly dividing cells, such as neoplastic lymphocytes.

Safety & warnings

Contraindications

  • Known hypersensitivity
  • Pre-existing bone marrow suppression
  • Liver dysfunction
  • Known pulmonary disease
  • Susceptibility to pulmonary fibrosis

Adverse effects

  • Myelosuppression
  • Gastrointestinal adverse events (including haemorrhagic gastroenteritis)
  • Liver enzyme activity elevation
  • Azotaemia
  • Fever
  • Weight loss
  • Lethargy
  • Dermatological signs
  • Pulmonary fibrosis
  • Injected sclera
  • Urinary signs (proteinuria, glycosuria)

Precautions

​Handling Precautions:​ Potent cytotoxic drug that should only be prepared and administered by trained personnel. See specialist texts for further advice on chemotherapeutic agents.

​Clinical Pearl:​ Extreme caution is advised regarding pulmonary toxicity; patients should be carefully screened for pre-existing lung conditions before initiating therapy.

Monitoring

  • Complete Blood Count (CBC) for myelosuppression
  • Liver enzyme activity
  • Renal parameters (BUN, Creatinine) and Urinalysis (for proteinuria/glycosuria)
  • Respiratory rate and effort (monitor for pulmonary fibrosis)
  • Clinical signs of gastrointestinal toxicity

Pharmacokinetics

Absorption

Administered intravenously; 100% bioavailability.

Distribution

Distributes to lymphoid tissues where it is loaded into target cells.

Metabolism

Acts as a prodrug; metabolized intracellularly to the active moiety PMEG and subsequently phosphorylated to the active PMEG diphosphate.

Elimination

Primarily eliminated via the kidneys.

Overdose

Information not provided in the monograph. Due to its cytotoxic nature, overdose is likely to cause severe myelosuppression, gastrointestinal toxicity, and potentially fatal pulmonary fibrosis. Aggressive supportive care and monitoring are indicated.

Available products

Formulations

  • Injectable: Sterile lyophilized powder for reconstitution (8.2 mg/ml after reconstitution)

Veterinary

  • Tanovea-CA1 (Sterile lyophilized powder)

Regulatory status

United States✓ ApprovedPrescription onlyFDA/CVM
🐕 Dogs

Initially conditionally approved as Tanovea-CA1, now fully approved as Tanovea.

European Union✗ Not approvedPrescription onlyEMA
🐕 Dogs

POM-V. Handled as a hazardous cytotoxic agent.

United Kingdom✗ Not approvedPrescription onlyVMD
🐕 Dogs

POM-V. Handled as a hazardous cytotoxic agent.

No regulatory data for: 🇭🇰 HK · 🇹🇼 TW · 🇯🇵 JP · 🇰🇷 KR · 🇦🇺 AU

Storage & stability

Sterile lyophilized powder for reconstitution before use. Reconstitute with 2 ml 0.9% NaCl.

Client information

Rabacfosadine is a chemotherapy drug used to treat certain types of cancer, like lymphoma, in dogs.

  • ​Handling waste:​ Because it is a chemotherapy drug, follow your veterinarian's instructions carefully regarding the handling of your dog's urine and feces for a few days after treatment.
  • ​What to watch for:​ Monitor your dog for signs of stomach upset (vomiting, diarrhea, loss of appetite), extreme tiredness, or any changes in breathing (like coughing or breathing heavily).
  • ​Breathing issues:​ > Contact your vet immediately if you notice any breathing difficulties, as this drug can rarely cause lung scarring (pulmonary fibrosis).

VetSheet drug reference is intended for licensed veterinary professionals as a clinical decision-support aid, not a substitute for professional judgement or the manufacturer’s current label.